Variant report

Variant	nsv429919
Chromosome Location	chr8:61771472-61979873
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3343)
CpG islands
(count:2872)
Chromatin interactive
region (count:126)
LncRNA
region (count:51)
Mature miRNA
region (count: 0)
miRNA target
sites (count:11)

(count:3343 , 50 per page) page: 1 2 3 4 5 6 7 ... 67

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:61936014-61936278	HepG2	liver:	n/a	n/a
2	ARID3A	chr8:61789676-61789708	K562	blood:	n/a	n/a
3	ARID3A	chr8:61821701-61821894	K562	blood:	n/a	n/a
4	ARID3A	chr8:61974821-61975024	K562	blood:	n/a	n/a
5	ARID3A	chr8:61926766-61927360	K562	blood:	n/a	n/a
6	ARID3A	chr8:61967152-61967655	K562	blood:	n/a	n/a
7	ARID3A	chr8:61968614-61968824	K562	blood:	n/a	n/a
8	ARID3A	chr8:61936071-61936274	K562	blood:	n/a	n/a
9	ARID3A	chr8:61862377-61862637	HepG2	liver:	n/a	n/a
10	ATF1	chr8:61966823-61967575	K562	blood:	n/a	n/a
11	ATF1	chr8:61974887-61975256	K562	blood:	n/a	n/a
12	ATF1	chr8:61824325-61824568	K562	blood:	n/a	n/a
13	ATF1	chr8:61926901-61927050	K562	blood:	n/a	n/a
14	ATF1	chr8:61863520-61863934	K562	blood:	n/a	n/a
15	ATF1	chr8:61893938-61894336	K562	blood:	n/a	n/a
16	ATF1	chr8:61838911-61839111	K562	blood:	n/a	n/a
17	ATF1	chr8:61968349-61968808	K562	blood:	n/a	n/a
18	ATF2	chr8:61821261-61822386	GM12878	blood:	n/a	n/a
19	ATF2	chr8:61911514-61912221	GM12878	blood:	n/a	n/a
20	ATF2	chr8:61859097-61859551	GM12878	blood:	n/a	n/a
21	ATF2	chr8:61870409-61870886	GM12878	blood:	n/a	n/a
22	ATF2	chr8:61821916-61822700	GM12878	blood:	n/a	n/a
23	ATF2	chr8:61815624-61817391	GM12878	blood:	n/a	n/a
24	ATF2	chr8:61823937-61825624	GM12878	blood:	n/a	n/a
25	ATF2	chr8:61828593-61829680	GM12878	blood:	n/a	n/a
26	ATF2	chr8:61828744-61829645	GM12878	blood:	n/a	n/a
27	ATF2	chr8:61863396-61863968	GM12878	blood:	n/a	n/a
28	ATF2	chr8:61838273-61838710	GM12878	blood:	n/a	n/a
29	ATF2	chr8:61891623-61892198	GM12878	blood:	n/a	n/a
30	ATF2	chr8:61838723-61840020	GM12878	blood:	n/a	n/a
31	ATF2	chr8:61822388-61822829	GM12878	blood:	n/a	n/a
32	ATF2	chr8:61841465-61842418	GM12878	blood:	n/a	n/a
33	ATF2	chr8:61841401-61842479	GM12878	blood:	n/a	n/a
34	ATF2	chr8:61823841-61825430	GM12878	blood:	n/a	n/a
35	ATF2	chr8:61815744-61817395	GM12878	blood:	n/a	n/a
36	ATF2	chr8:61911577-61912193	GM12878	blood:	n/a	n/a
37	ATF2	chr8:61859704-61860235	GM12878	blood:	n/a	n/a
38	ATF2	chr8:61859562-61860359	GM12878	blood:	n/a	n/a
39	ATF2	chr8:61863437-61864041	GM12878	blood:	n/a	n/a
40	ATF2	chr8:61838738-61839676	GM12878	blood:	n/a	n/a
41	ATF3	chr8:61926783-61927119	K562	blood:	n/a	n/a
42	ATF3	chr8:61966047-61966345	K562	blood:	n/a	n/a
43	BACH1	chr8:61966729-61966906	K562	blood:	n/a	n/a
44	BACH1	chr8:61824664-61824827	H1-hESC	embryonic stem cell:	n/a	n/a
45	BACH1	chr8:61822386-61822580	H1-hESC	embryonic stem cell:	n/a	n/a
46	BACH1	chr8:61834052-61834461	H1-hESC	embryonic stem cell:	n/a	n/a
47	BACH1	chr8:61967219-61967247	K562	blood:	n/a	n/a
48	BACH1	chr8:61835323-61835552	H1-hESC	embryonic stem cell:	n/a	n/a
49	BACH1	chr8:61834885-61835038	H1-hESC	embryonic stem cell:	n/a	n/a
50	BACH1	chr8:61936368-61936627	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2872 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61787436-61787486	AG09319	gingival:	n/a
2	chr8:61835708-61835758	HCF	heart:	n/a
3	chr8:61789727-61789777	AG09319	gingival:	n/a
4	chr8:61861713-61861763	Hela-S3	cervix:	n/a
5	chr8:61778137-61778187	HAEpiC	amniotic membrane:	n/a
6	chr8:61787436-61787486	AG09319	gingival:	n/a
7	chr8:61835708-61835758	HCF	heart:	n/a
8	chr8:61789727-61789777	AG09319	gingival:	n/a
9	chr8:61861713-61861763	Hela-S3	cervix:	n/a
10	chr8:61778137-61778187	HAEpiC	amniotic membrane:	n/a
11	chr8:61926269-61926319	GM12891	blood:	n/a
12	chr8:61926269-61926319	SAEC	small airway:	n/a
13	chr8:61778137-61778187	HRCEpiC	kidney:	n/a
14	chr8:61823027-61823077	Hepatocyte	liver:	n/a
15	chr8:61880392-61880442	HCPEpiC	choroid plexus:	n/a
16	chr8:61835175-61835225	HEK293	kidney:	embryo
17	chr8:61837048-61837098	A549	lung:	n/a
18	chr8:61917230-61917280	HAEpiC	amniotic membrane:	n/a
19	chr8:61818850-61818900	HMEC	breast:	n/a
20	chr8:61789834-61789884	NHDF-neo	bronchial:	n/a
21	chr8:61821400-61821450	PrEC	prostate:	n/a
22	chr8:61823275-61823325	HIPEpiC	eye:	n/a
23	chr8:61861713-61861763	AG04450	lung:	fetal
24	chr8:61789893-61789943	HEEpiC	esophagus:	n/a
25	chr8:61917230-61917280	SAEC	small airway:	n/a
26	chr8:61835620-61835670	MCF10A-Er-Src	breast:	n/a
27	chr8:61785026-61785076	AG04449	skin:	fetal
28	chr8:61778137-61778187	GM12878	blood:	n/a
29	chr8:61789011-61789061	ProgFib	skin:	n/a
30	chr8:61789893-61789943	AG09309	skin:	n/a
31	chr8:61778137-61778187	U87	brain:	n/a
32	chr8:61835620-61835670	AG04449	skin:	fetal
33	chr8:61874908-61874958	MCF10A-Er-Src	breast:	n/a
34	chr8:61785026-61785076	SK-N-SH	brain:	n/a
35	chr8:61835119-61835169	GM12891	blood:	n/a
36	chr8:61874021-61874071	HCF	heart:	n/a
37	chr8:61778137-61778187	T-47D	breast:	n/a
38	chr8:61777765-61777815	LNCaP	prostate:	n/a
39	chr8:61835620-61835670	PFSK-1	brain:	n/a
40	chr8:61874021-61874071	SK-N-MC	brain:	n/a
41	chr8:61789893-61789943	GM12892	blood:	n/a
42	chr8:61834943-61834993	A549	lung:	n/a
43	chr8:61880392-61880442	ProgFib	skin:	n/a
44	chr8:61789077-61789127	T-47D	breast:	n/a
45	chr8:61936333-61936383	GM12878	blood:	n/a
46	chr8:61777765-61777815	HRE	kidney:	n/a
47	chr8:61834943-61834993	Jurkat	blood:	n/a
48	chr8:61863697-61863747	AoSMC	blood vessel:	n/a
49	chr8:61917230-61917280	BJ	skin:	n/a
50	chr8:61789893-61789943	SK-N-SH	brain:	n/a

(count:126 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr8:61909390..61914043-chr8:61914275..61917284,4	K562	blood:
2	chr8:61904064..61906446-chr8:61914213..61915815,2	K562	blood:
3	chr8:61804411..61807326-chr8:61808389..61811316,2	K562	blood:
4	chr8:61931901..61935171-chr8:61938511..61943080,4	K562	blood:
5	chr8:61909286..61911091-chr8:61912763..61914485,2	K562	blood:
6	chr8:61887957..61892513-chr8:61893638..61896682,5	K562	blood:
7	chr8:61940028..61943357-chr8:61945337..61947792,3	MCF-7	breast:
8	chr8:61812523..61815203-chr8:61818659..61820454,2	MCF-7	breast:
9	chr8:61939184..61941234-chr8:61941938..61944773,2	K562	blood:
10	chr8:61931901..61935171-chr8:61938511..61943080,4	K562	blood:
11	chr8:61790307..61792486-chr8:61807700..61810532,2	K562	blood:
12	chr8:61963224..61963734-chr8:62008381..62008913,2	MCF-7	breast:
13	chr8:61967667..61969481-chr8:61970282..61972656,2	MCF-7	breast:
14	chr8:61926425..61928022-chr8:61931862..61934315,2	K562	blood:
15	chr8:61821654..61824637-chr8:61859951..61861851,2	MCF-7	breast:
16	chr8:61779349..61781362-chr8:61781612..61783188,2	MCF-7	breast:
17	chr8:61559948..61562739-chr8:61935074..61937781,2	K562	blood:
18	chr8:61681827..61683875-chr8:61893342..61894850,2	MCF-7	breast:
19	chr8:61915782..61918089-chr8:61971663..61974178,2	K562	blood:
20	chr8:61853213..61856894-chr8:61860542..61864181,3	MCF-7	breast:
21	chr8:61952051..61954577-chr8:61966182..61967998,2	K562	blood:
22	chr8:61926425..61928022-chr8:61931862..61934315,2	K562	blood:
23	chr1:45187059..45187602-chr8:61961283..61961803,2	Hela-S3	cervix:
24	chr8:61916700..61920504-chr8:61923815..61926099,3	K562	blood:
25	chr8:61854686..61856226-chr8:61860743..61862547,2	K562	blood:
26	chr8:61835952..61838593-chr8:61841536..61843319,2	K562	blood:
27	chr8:61925781..61927667-chr8:61931252..61932864,2	MCF-7	breast:
28	chr8:61806847..61808765-chr8:61810368..61811960,2	MCF-7	breast:
29	chr8:61893041..61895787-chr8:61898725..61901376,3	K562	blood:
30	chr8:61933739..61936332-chr8:61953830..61956057,2	MCF-7	breast:
31	chr8:61790307..61792486-chr8:61807700..61810532,2	K562	blood:
32	chr8:61946643..61952580-chr8:61954508..61959769,7	K562	blood:
33	chr8:61573025..61573694-chr8:61935940..61936504,2	MCF-7	breast:
34	chr8:61873885..61874676-chr8:62008576..62009223,2	K562	blood:
35	chr8:61935230..61937011-chr8:61938977..61940542,2	K562	blood:
36	chr8:61562777..61567370-chr8:61946325..61952139,6	K562	blood:
37	chr8:61922784..61924643-chr8:61937030..61939869,2	MCF-7	breast:
38	chr8:61837800..61840133-chr8:61855900..61858739,2	MCF-7	breast:
39	chr8:61798544..61800476-chr8:61802486..61805263,2	MCF-7	breast:
40	chr8:61563900..61565522-chr8:61931938..61933624,2	MCF-7	breast:
41	chr8:61851365..61853234-chr8:61857166..61859095,2	K562	blood:
42	chr8:61937931..61939509-chr8:61940815..61942936,2	MCF-7	breast:
43	chr8:61961512..61964548-chr8:61967197..61971349,3	K562	blood:
44	chr8:61833393..61835829-chr8:61842077..61844406,2	K562	blood:
45	chr8:61829988..61832075-chr8:61833915..61836317,2	K562	blood:
46	chr8:61854686..61856226-chr8:61860743..61862547,2	K562	blood:
47	chr8:61849973..61853461-chr8:61859040..61861744,3	MCF-7	breast:
48	chr8:61940028..61943357-chr8:61945337..61947792,3	MCF-7	breast:
49	chr8:61806847..61808765-chr8:61810368..61811960,2	MCF-7	breast:
50	chr8:61926018..61928553-chr8:61929575..61931127,2	K562	blood:

(count:51 , 50 per page) page: 1 2

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASPH-5	chr8:61878682-61879016	XLOC_007097
2	lnc-CLVS1-1	chr8:61877795-61877920	NONHSAT126853
3	lnc-CLVS1-1	chr8:61939695-61940021	XLOC_006815
4	lnc-CLVS1-1	chr8:61874529-61875010	NONHSAT126853
5	lnc-CLVS1-1	chr8:61865489-61865594	ENSG00000254777
6	lnc-CLVS1-1	chr8:61822245-61822787	NONHSAT126853
7	lnc-CLVS1-1	chr8:61875911-61875984	ENSG00000254777
8	lnc-CLVS1-1	chr8:61865488-61865594	NONHSAT126853
9	lnc-ASPH-5	chr8:61880132-61880323	NONHSAT126857
10	lnc-ASPH-5	chr8:61880132-61880334	ENSG00000254802
11	lnc-CLVS1-1	chr8:61880132-61880307	NONHSAT126853
12	lnc-CLVS1-1	chr8:61878746-61878796	XLOC_006815
13	lnc-ASPH-5	chr8:61878361-61879016	ENSG00000254802
14	lnc-ASPH-5	chr8:61878680-61879016	NR_034003
15	lnc-CHD7-2	chr8:61781100-61783405	NONHSAT126850
16	lnc-CLVS1-1	chr8:61878729-61879015	ENSG00000254777
17	lnc-ASPH-6	chr8:61822077-61822321	XLOC_007096
18	lnc-CLVS1-1	chr8:61877289-61877382	ENSG00000254777
19	lnc-CLVS1-1	chr8:61812992-61813052	NONHSAT126851
20	lnc-CLVS1-1	chr8:61822612-61822787	ENSG00000254777
21	lnc-CLVS1-1	chr8:61831540-61831609	ENSG00000254777
22	lnc-CLVS1-1	chr8:61877116-61877641	NONHSAT126853
23	lnc-ASPH-5	chr8:61880132-61880307	NR_034003
24	lnc-CLVS1-1	chr8:61831540-61835815	NONHSAT126851
25	lnc-ASPH-5	chr8:61877666-61879016	NONHSAT126857
26	lnc-CLVS1-4	chr8:61936148-61936900	NONHSAT126860
27	lnc-CLVS1-1	chr8:61875910-61875992	NONHSAT126853
28	lnc-CLVS1-1	chr8:61939695-61940024	XLOC_006815
29	lnc-CLVS1-1	chr8:61832729-61832981	NONHSAT126853
30	lnc-CLVS1-1	chr8:61878729-61879017	NONHSAT126853
31	lnc-CLVS1-1	chr8:61879030-61879056	NONHSAT126853
32	lnc-CLVS1-1	chr8:61877796-61877920	ENSG00000254777
33	lnc-CLVS1-1	chr8:61847014-61847227	NONHSAT126853
34	lnc-CLVS1-1	chr8:61878733-61879116	ENSG00000254777
35	lnc-CLVS1-1	chr8:61873549-61874008	NONHSAT126853
36	lnc-CLVS1-1	chr8:61832729-61832981	ENSG00000254777
37	lnc-CLVS1-1	chr8:61877289-61877382	ENSG00000254777
38	lnc-CLVS1-1	chr8:61879073-61879112	NONHSAT126853
39	lnc-ASPH-6	chr8:61823051-61823092	XLOC_007096
40	lnc-CLVS1-1	chr8:61936025-61936049	XLOC_006815
41	lnc-CLVS1-1	chr8:61823149-61823225	ENSG00000254777
42	lnc-CLVS1-1	chr8:61838352-61838934	NONHSAT126853
43	lnc-CLVS1-1	chr8:61832729-61832981	ENSG00000254777
44	lnc-CLVS1-1	chr8:61938094-61938819	NONHSAT126853
45	lnc-CLVS1-1	chr8:61850156-61850643	NONHSAT126853
46	lnc-CLVS1-1	chr8:61823149-61823225	NONHSAT126853
47	lnc-CLVS1-1	chr8:61888688-61889223	NONHSAT126853
48	lnc-CLVS1-1	chr8:61831539-61831609	NONHSAT126853
49	lnc-CLVS1-1	chr8:61831540-61831609	ENSG00000254777
50	lnc-CLVS1-1	chr8:61897734-61898214	NONHSAT126853

No data

(count:11 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CHD7	hsa-miR-98-5p	chr8:61779279-61779285
2	CHD7	hsa-let-7b-5p	chr8:61779279-61779285
3	CHD7	hsa-miR-192-5p	chr8:61779825-61779831
4	CHD7	hsa-let-7b-5p	chr8:61779266-61779285
5	CHD7	hsa-miR-192-5p	chr8:61778905-61778911
6	CHD7	hsa-miR-215-5p	chr8:61778905-61778911
7	CHD7	hsa-miR-98-5p	chr8:61779266-61779285
8	CHD7	hsa-let-7e-5p	chr8:61779279-61779285
9	CHD7	hsa-miR-215-5p	chr8:61779825-61779831
10	CHD7	hsa-let-7e-5p	chr8:61779263-61779285
11	CHD7	hsa-miR-454-3p	chr8:61779146-61779168

Variant related genes	Relation type
CLVS1	TF binding region
ENSG00000255397	TF binding region
CHD7	TF binding region
ENSG00000271377	TF binding region
ENSG00000254777	TF binding region
ENSG00000254802	TF binding region
CLVS1	CpG island
ENSG00000255397	CpG island
CHD7	CpG island
ENSG00000271377	CpG island
ENSG00000254777	CpG island
ENSG00000254802	CpG island
ENSG00000254777	chromatin interactions
ENSG00000255289	chromatin interactions
ENSG00000254869	chromatin interactions
ENSG00000177182	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000255397	chromatin interactions
ENSG00000171316	chromatin interactions
HECTD3	miRNA target sites
ATP1A2	miRNA target sites

Extended variants
information (count: 7944 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:7944 , 50 per page) page: 1 2 3 4 5 6 7 ... 159

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13256570	chr8:61771472-61771473	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566968802	chr8:61771507-61771508	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182265777	chr8:61771524-61771525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115783053	chr8:61771528-61771529	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572408282	chr8:61771599-61771600	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs567630927	chr8:61771600-61771601	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538180993	chr8:61771618-61771619	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534990696	chr8:61771634-61771635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186517864	chr8:61771676-61771677	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs34162663	chr8:61771697-61771698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs189774096	chr8:61771745-61771746	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs539215023	chr8:61771753-61771754	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs142635600	chr8:61771792-61771793	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs182466425	chr8:61771796-61771797	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs145943863	chr8:61771797-61771798	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs577997098	chr8:61771825-61771826	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs13257536	chr8:61771835-61771836	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs563855208	chr8:61771896-61771897	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs573873947	chr8:61771908-61771909	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs138505880	chr8:61772039-61772040	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561864194	chr8:61772040-61772041	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs116431079	chr8:61772050-61772051	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185700972	chr8:61772108-61772109	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs551532048	chr8:61772153-61772154	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs560602778	chr8:61772154-61772155	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs114797818	chr8:61772185-61772186	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149271400	chr8:61772191-61772192	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs567669719	chr8:61772235-61772236	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs538200426	chr8:61772240-61772241	Weak transcription Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs550251219	chr8:61772371-61772372	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35839790	chr8:61772373-61772374	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs144494358	chr8:61772382-61772383	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs116303687	chr8:61772412-61772413	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191248027	chr8:61772455-61772456	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572269776	chr8:61772500-61772501	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs114836380	chr8:61772504-61772505	Weak transcription Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs553022251	chr8:61772557-61772558	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs554996451	chr8:61772570-61772571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs112874128	chr8:61772586-61772587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs573565697	chr8:61772596-61772597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs544185420	chr8:61772625-61772626	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs529529415	chr8:61772735-61772736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs562668797	chr8:61772763-61772764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs528409626	chr8:61772801-61772802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375755298	chr8:61772812-61772813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577853246	chr8:61772831-61772832	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544942111	chr8:61772836-61772837	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148570368	chr8:61772863-61772864	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs16926514	chr8:61772899-61772900	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs183049367	chr8:61772983-61772984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Salivary gland tumor	18059337	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ependymoma	20639864	CNVD
Colorectal cancer	21645411	CNVD
Charge syndrome	20571795	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Sezary syndrome	18413736	CNVD

Chromatin state (count:5042 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61718800-61781000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:61740400-61780200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr8:61741800-61777600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr8:61741800-61780800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr8:61742200-61778800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr8:61743400-61777400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr8:61748400-61771800	Strong transcription	HUES48 Cell Line	embryonic stem cell
8	chr8:61749400-61777600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
9	chr8:61750800-61776200	Strong transcription	Liver	Liver
10	chr8:61751000-61777800	Weak transcription	Aorta	Aorta
11	chr8:61751800-61780400	Strong transcription	Fetal Intestine Large	intestine
12	chr8:61752600-61780400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
13	chr8:61752800-61773800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr8:61752800-61779000	Strong transcription	iPS-20b Cell Line	embryonic stem cell
15	chr8:61753000-61779200	Strong transcription	HUES64 Cell Line	embryonic stem cell
16	chr8:61753200-61779400	Strong transcription	HUES6 Cell Line	embryonic stem cell
17	chr8:61753200-61782000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr8:61753400-61772400	Strong transcription	Dnd41	blood
19	chr8:61753600-61778600	Strong transcription	Duodenum Mucosa	Duodenum
20	chr8:61759600-61776400	Strong transcription	Primary T cells from cord blood	blood
21	chr8:61760400-61780000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr8:61760400-61780400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr8:61761000-61777800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr8:61761000-61778600	Strong transcription	Sigmoid Colon	Sigmoid Colon
25	chr8:61761000-61780600	Strong transcription	Primary B cells from peripheral blood	blood
26	chr8:61762200-61776200	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr8:61762400-61779400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr8:61762600-61772400	Strong transcription	Rectal Mucosa Donor 31	rectum
29	chr8:61763200-61772200	Strong transcription	Fetal Thymus	thymus
30	chr8:61764400-61780400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr8:61765000-61775800	Weak transcription	Right Atrium	heart
32	chr8:61765000-61780600	Weak transcription	Stomach Mucosa	stomach
33	chr8:61765000-61780800	Strong transcription	Primary B cells from cord blood	blood
34	chr8:61765200-61778800	Strong transcription	Fetal Lung	lung
35	chr8:61765800-61777200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
36	chr8:61766000-61775600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr8:61766200-61772000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr8:61766200-61777600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chr8:61766800-61776800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr8:61767000-61773600	Weak transcription	Placenta Amnion	Placenta Amnion
41	chr8:61767000-61777000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
42	chr8:61767000-61777400	Strong transcription	HSMM	muscle
43	chr8:61767200-61777200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
44	chr8:61768000-61772200	Strong transcription	HSMMtube	muscle
45	chr8:61768000-61772400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:61768000-61774200	Strong transcription	Fetal Intestine Small	intestine
47	chr8:61768000-61778800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
48	chr8:61768600-61771800	Strong transcription	Brain Anterior Caudate	brain
49	chr8:61768800-61771600	Weak transcription	Thymus	Thymus
50	chr8:61769200-61771800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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