Variant report

Variant	nsv519768
Chromosome Location	chr8:10600254-10691993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1878)
CpG islands
(count:1404)
Chromatin interactive
region (count:93)
LncRNA
region (count:11)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1878 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:10676462-10676890	K562	blood:	n/a	n/a
2	ARID3A	chr8:10632964-10633416	K562	blood:	n/a	n/a
3	ARID3A	chr8:10629194-10629470	K562	blood:	n/a	n/a
4	ARID3A	chr8:10657288-10657802	K562	blood:	n/a	n/a
5	ARID3A	chr8:10631175-10631647	K562	blood:	n/a	n/a
6	ARID3A	chr8:10653397-10654025	K562	blood:	n/a	n/a
7	ARID3A	chr8:10657152-10657846	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:10618425-10619055	K562	blood:	n/a	n/a
9	ARID3A	chr8:10638845-10638952	K562	blood:	n/a	n/a
10	ARID3A	chr8:10656082-10656601	K562	blood:	n/a	n/a
11	ARID3A	chr8:10634540-10635222	K562	blood:	n/a	n/a
12	ARID3A	chr8:10665773-10666115	K562	blood:	n/a	n/a
13	ATF1	chr8:10634783-10635469	K562	blood:	n/a	n/a
14	ATF1	chr8:10671700-10671979	K562	blood:	n/a	n/a
15	ATF1	chr8:10629162-10629538	K562	blood:	n/a	n/a
16	ATF1	chr8:10653494-10654054	K562	blood:	n/a	n/a
17	ATF1	chr8:10657290-10657727	K562	blood:	n/a	n/a
18	ATF1	chr8:10618426-10618829	K562	blood:	n/a	n/a
19	ATF2	chr8:10641139-10641593	GM12878	blood:	n/a	n/a
20	ATF2	chr8:10646115-10646583	GM12878	blood:	n/a	n/a
21	ATF2	chr8:10641097-10641653	GM12878	blood:	n/a	n/a
22	ATF2	chr8:10646076-10646653	GM12878	blood:	n/a	n/a
23	ATF3	chr8:10634812-10635209	K562	blood:	n/a	n/a
24	ATF3	chr8:10657250-10657724	K562	blood:	n/a	n/a
25	ATF3	chr8:10657391-10657631	K562	blood:	n/a	n/a
26	BACH1	chr8:10634535-10634552	K562	blood:	n/a	n/a
27	BACH1	chr8:10618657-10618682	K562	blood:	n/a	n/a
28	BACH1	chr8:10676446-10676803	K562	blood:	n/a	n/a
29	BATF	chr8:10663103-10663760	GM12878	blood:	n/a	n/a
30	BATF	chr8:10646148-10646551	GM12878	blood:	n/a	chr8:10646312-10646323
31	BATF	chr8:10641195-10641508	GM12878	blood:	n/a	chr8:10641369-10641380
32	BATF	chr8:10641154-10641577	GM12878	blood:	n/a	chr8:10641369-10641380
33	BCL11A	chr8:10646180-10646518	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:10663503-10663756	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:10641274-10641544	GM12878	blood:	n/a	n/a
36	BCL3	chr8:10646199-10646599	GM12878	blood:	n/a	n/a
37	BHLHE40	chr8:10629130-10629563	K562	blood:	n/a	n/a
38	BHLHE40	chr8:10675975-10676782	K562	blood:	n/a	chr8:10676166-10676175 chr8:10676166-10676175 chr8:10676160-10676181 chr8:10676525-10676541 chr8:10676165-10676174
39	BHLHE40	chr8:10634083-10635624	K562	blood:	n/a	n/a
40	BHLHE40	chr8:10653533-10653798	K562	blood:	n/a	n/a
41	BHLHE40	chr8:10646418-10646431	K562	blood:	n/a	n/a
42	BHLHE40	chr8:10618383-10618969	K562	blood:	n/a	n/a
43	BHLHE40	chr8:10633148-10633444	K562	blood:	n/a	n/a
44	BHLHE40	chr8:10648112-10648199	K562	blood:	n/a	n/a
45	BHLHE40	chr8:10657309-10657639	K562	blood:	n/a	n/a
46	BHLHE40	chr8:10682842-10683140	GM12878	blood:	n/a	n/a
47	BRCA1	chr8:10682855-10683017	GM12878	blood:	n/a	n/a
48	BRCA1	chr8:10647677-10647797	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr8:10645582-10645644	Hela-S3	cervix:	n/a	n/a
50	BRCA1	chr8:10657228-10657844	Hela-S3	cervix:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:10657514-10657564	SAEC	small airway:	n/a
2	chr8:10657514-10657564	SAEC	small airway:	n/a
3	chr8:10621935-10621985	HUVEC	blood vessel:	n/a
4	chr8:10683044-10683094	HMEC	breast:	n/a
5	chr8:10621801-10621851	HAEpiC	amniotic membrane:	n/a
6	chr8:10686070-10686120	AG04449	skin:	fetal
7	chr8:10622805-10622855	HAEpiC	amniotic membrane:	n/a
8	chr8:10623534-10623584	SAEC	small airway:	n/a
9	chr8:10621801-10621851	PANC-1	pancreas:	n/a
10	chr8:10650046-10650096	HAEpiC	amniotic membrane:	n/a
11	chr8:10623038-10623088	MCF10A-Er-Src	breast:	n/a
12	chr8:10683139-10683189	GM12878	blood:	n/a
13	chr8:10622805-10622855	HPAEpiC	pulmonary alveolar:	n/a
14	chr8:10621935-10621985	PANC-1	pancreas:	n/a
15	chr8:10621801-10621851	IMR90	lung:	fetal
16	chr8:10623038-10623088	AG04449	skin:	fetal
17	chr8:10621801-10621851	NH-A	brain:	n/a
18	chr8:10643634-10643684	HCPEpiC	choroid plexus:	n/a
19	chr8:10621874-10621924	ECC-1	luminal epithelium:	n/a
20	chr8:10617394-10617444	HAEpiC	amniotic membrane:	n/a
21	chr8:10622805-10622855	HNPCEpiC	eye:	n/a
22	chr8:10650046-10650096	AoSMC	blood vessel:	n/a
23	chr8:10649960-10650010	A549	lung:	n/a
24	chr8:10623038-10623088	K562	blood:	n/a
25	chr8:10683044-10683094	HepG2	liver:	n/a
26	chr8:10683266-10683316	LNCaP	prostate:	n/a
27	chr8:10683266-10683316	NB4	blood:	n/a
28	chr8:10649960-10650010	NB4	blood:	n/a
29	chr8:10622887-10622937	GM19239	blood:	n/a
30	chr8:10683044-10683094	GM12878	blood:	n/a
31	chr8:10621801-10621851	T-47D	breast:	n/a
32	chr8:10683266-10683316	GM12878	blood:	n/a
33	chr8:10621935-10621985	AG04449	skin:	fetal
34	chr8:10657514-10657564	SKMC	muscle:	n/a
35	chr8:10683044-10683094	SKMC	muscle:	n/a
36	chr8:10683167-10683217	HIPEpiC	eye:	n/a
37	chr8:10623038-10623088	GM12891	blood:	n/a
38	chr8:10657514-10657564	GM12891	blood:	n/a
39	chr8:10683188-10683238	HIPEpiC	eye:	n/a
40	chr8:10683139-10683189	NHDF-neo	bronchial:	n/a
41	chr8:10683266-10683316	K562	blood:	n/a
42	chr8:10621874-10621924	HepG2	liver:	n/a
43	chr8:10650046-10650096	BJ	skin:	n/a
44	chr8:10643634-10643684	H1-hESC	embryonic stem cell:	embryo
45	chr8:10646690-10646740	SK-N-SH	brain:	n/a
46	chr8:10622887-10622937	Hela-S3	cervix:	n/a
47	chr8:10657514-10657564	AG10803	skin:	n/a
48	chr8:10657514-10657564	GM19239	blood:	n/a
49	chr8:10621801-10621851	HPAEpiC	pulmonary alveolar:	n/a
50	chr8:10622887-10622937	MCF10A-Er-Src	breast:	n/a

(count:93 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:10631743..10634256-chr8:10658449..10660185,2	K562	blood:
2	chr8:10407992..10408718-chr8:10682226..10683074,2	MCF-7	breast:
3	chr8:10671204..10673781-chr8:10675039..10678414,4	K562	blood:
4	chr8:10447282..10448390-chr8:10682147..10683493,10	MCF-7	breast:
5	chr8:10615706..10617702-chr8:10620374..10622044,2	K562	blood:
6	chr8:10444435..10445487-chr8:10682600..10683390,5	MCF-7	breast:
7	chr8:10621941..10624619-chr8:10627842..10631333,3	K562	blood:
8	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
9	chr8:10444578..10445174-chr8:10671828..10672358,2	MCF-7	breast:
10	chr8:10683547..10686608-chr8:10694341..10697878,5	K562	blood:
11	chr8:10444886..10445502-chr8:10682512..10683360,2	MCF-7	breast:
12	chr8:10613644..10615982-chr8:10616006..10618005,2	MCF-7	breast:
13	chr8:10687156..10690707-chr8:10693616..10698468,7	K562	blood:
14	chr8:10447388..10448227-chr8:10671479..10672292,5	MCF-7	breast:
15	chr8:10622933..10625831-chr8:10627358..10629898,3	K562	blood:
16	chr8:10674524..10677009-chr8:10677940..10682794,6	K562	blood:
17	chr8:10447726..10448226-chr8:10680360..10680981,2	K562	blood:
18	chr8:10647998..10650941-chr8:10651803..10654879,3	K562	blood:
19	chr8:10635373..10637028-chr8:10639267..10640869,2	MCF-7	breast:
20	chr8:10674524..10677009-chr8:10677940..10680830,2	K562	blood:
21	chr8:10595931..10598685-chr8:10600314..10603281,2	K562	blood:
22	chr8:10640744..10643813-chr8:10646247..10648006,3	K562	blood:
23	chr8:10533955..10536464-chr8:10664070..10665725,2	K562	blood:
24	chr8:10515210..10517092-chr8:10648053..10650432,2	K562	blood:
25	chr8:10655273..10657441-chr8:10673003..10675779,2	MCF-7	breast:
26	chr8:10654838..10657527-chr8:10667570..10669417,2	K562	blood:
27	chr8:10663898..10666534-chr8:10670905..10672921,2	K562	blood:
28	chr8:10670666..10672714-chr8:10674903..10676605,2	K562	blood:
29	chr8:10659319..10661970-chr8:10670204..10672080,2	K562	blood:
30	chr8:10634439..10636776-chr8:10637920..10639941,2	K562	blood:
31	chr8:10412812..10415531-chr8:10671274..10673611,2	K562	blood:
32	chr8:10517902..10518777-chr8:10655034..10655826,2	K562	blood:
33	chr8:10655273..10657441-chr8:10673003..10675779,2	MCF-7	breast:
34	chr8:10651485..10654382-chr8:10658663..10661335,2	K562	blood:
35	chr8:10648353..10650941-chr8:10651549..10653303,2	K562	blood:
36	chr8:10690421..10694581-chr8:10695821..10698975,5	MCF-7	breast:
37	chr8:10620237..10621942-chr8:10624836..10626716,2	K562	blood:
38	chr8:10616130..10621063-chr8:10631004..10634975,5	K562	blood:
39	chr8:10622933..10625831-chr8:10627358..10629898,3	K562	blood:
40	chr8:10647998..10650941-chr8:10651803..10654879,3	K562	blood:
41	chr8:10633410..10636281-chr8:10695946..10698229,2	K562	blood:
42	chr8:10674954..10678350-chr8:10693952..10697087,3	K562	blood:
43	chr8:10674524..10677009-chr8:10677940..10682794,6	K562	blood:
44	chr8:10644063..10645864-chr8:10646300..10647918,2	K562	blood:
45	chr8:10611693..10613429-chr8:10616715..10619425,2	K562	blood:
46	chr8:10648269..10650512-chr8:10653379..10655643,2	K562	blood:
47	chr8:10687146..10690339-chr8:10690695..10692954,3	K562	blood:
48	chr8:10615706..10617702-chr8:10620374..10622044,2	K562	blood:
49	chr8:10615290..10617626-chr8:10678525..10680394,2	K562	blood:
50	chr8:10637227..10639658-chr8:10641198..10643629,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C8orf74-1	chr8:10628705-10628902	ENSG00000248896
2	lnc-C8orf74-1	chr8:10621847-10622667	NONHSAT125014
3	lnc-C8orf74-1	chr8:10622680-10622686	NONHSAT125014
4	lnc-PINX1-1	chr8:10615296-10618693	NONHSAT125016
5	lnc-C8orf74-4	chr8:10659257-10660077	ucscGeneNc_uc003wtg_1
6	lnc-RP1L1-7	chr8:10660588-10662320	NONHSAT125018
7	lnc-C8orf74-4	chr8:10649122-10649238	ucscGeneNc_uc003wtg_1
8	lnc-C8orf74-1	chr8:10621847-10622233	ENSG00000248896
9	lnc-C8orf74-4	chr8:10624234-10624550	ucscGeneNc_uc003wtg_1
10	lnc-C8orf74-1	chr8:10611712-10611828	NONHSAT125014
11	lnc-C8orf74-1	chr8:10611712-10611828	ENSG00000248896

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1322	chr8:10682885-10682903	MIMAT0005953

No data

Variant related genes	Relation type
ENSG00000252565	TF binding region
PINX1	TF binding region
ENSG00000252565	CpG island
PINX1	CpG island
ENSG00000258724	chromatin interactions
ENSG00000252565	chromatin interactions
ENSG00000254093	chromatin interactions
ENSG00000253695	chromatin interactions
HSPA1B	miRNA target sites

Extended variants
information (count: 4820 )
Associated
traits (count: 149 )

Variant overlapped rSNPs/rCNVs (count:4820 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563324643	chr8:10607817-10607818	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs528842176	chr8:10607818-10607819	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs548511765	chr8:10607821-10607822	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs146695449	chr8:10607839-10607840	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs57076989	chr8:10607906-10607907	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs71516592	chr8:10607907-10607908	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs181696535	chr8:10607953-10607954	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs539891715	chr8:10607984-10607985	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs536243945	chr8:10608019-10608020	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs549982905	chr8:10608026-10608027	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs556619359	chr8:10608055-10608056	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs186350181	chr8:10608064-10608065	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs539406327	chr8:10608091-10608092	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs535849083	chr8:10608105-10608106	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs555705611	chr8:10608141-10608142	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs565941664	chr8:10608146-10608147	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs534535397	chr8:10608173-10608174	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs189936362	chr8:10608176-10608177	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs577742448	chr8:10608178-10608179	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs75001032	chr8:10608182-10608183	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs556771542	chr8:10608226-10608227	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs573348151	chr8:10608233-10608234	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs542167573	chr8:10608280-10608281	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs562053230	chr8:10608299-10608300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs117859815	chr8:10608323-10608324	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs114732302	chr8:10608329-10608330	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs564727217	chr8:10608343-10608344	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs533344597	chr8:10608356-10608357	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs58297791	chr8:10608359-10608360	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs181157947	chr8:10608371-10608372	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs529316622	chr8:10608381-10608382	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs111378698	chr8:10608387-10608388	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs549365069	chr8:10608409-10608410	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs566002580	chr8:10608419-10608420	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs541694195	chr8:10608421-10608422	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs534947827	chr8:10608459-10608460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs59421673	chr8:10608490-10608491	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs557752407	chr8:10608536-10608537	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs112256810	chr8:10608568-10608569	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs571459884	chr8:10608573-10608574	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs536850836	chr8:10608581-10608582	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs560769910	chr8:10608595-10608596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs140338895	chr8:10608608-10608609	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs373187739	chr8:10608615-10608616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs375831110	chr8:10608635-10608636	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs573360323	chr8:10608677-10608678	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs542228414	chr8:10608742-10608743	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs145496417	chr8:10608766-10608767	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs572481019	chr8:10608835-10608836	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs541741366	chr8:10608838-10608839	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:149)

Disease	PMID	Source
Crohn''s disease	19220326	CNVD
Psoriasis	19220326	CNVD
Prostate cancer	21965145	CNVD
Prostate cancer	18515986	CNVD
Chronic obstructive pulmonary disease	20378733	CNVD
Autism	18414403	CNVD
Cancer	21183584	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	17603634	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Ovarian cancer	20844748	CNVD
Cervical cancer	17311676	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Schizophrenia	20877625	CNVD
Disorders of sex development	21048976	CNVD
Colorectal cancer	16272173	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	17001317	CNVD
Thyroid cancer	19087340	CNVD
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	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
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21064195	CNVD
Autism	22495311	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	21990379	CNVD
Psoriasis	20403174	CNVD
Psoriasis	20663923	CNVD
Crohn''s disease	16909382	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Crohn''s disease	20877625	CNVD
Inflammatory disorder	20877625	CNVD
Cardiac defect	21933911	CNVD
Psoriasis	18059266	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Psoriasis	20877625	CNVD
Mental retardation	17847001	CNVD
Prostate cancer	17217626	CNVD
Schizophrenia	21399695	CNVD
Colorectal cancer	21128281	CNVD
Colorectal cancer	19455253	CNVD
Psoriasis	18848619	CNVD
Squamous cell cancer	19047905	CNVD
Colorectal cancer	17229543	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Developmental disorder	20461109	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Glioblastoma multiforme	21138945	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Gastric cancer	21811585	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Osteosarcoma	21215367	CNVD
Schizophrenia	23813976	CNVD
Autism	20531469	CNVD

Chromatin state (count:2281 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:10607800-10609400	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
2	chr8:10609600-10610000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr8:10609600-10610000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
4	chr8:10609600-10614000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr8:10609600-10616200	Weak transcription	Primary T cells from cord blood	blood
6	chr8:10610000-10621400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr8:10610200-10610400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr8:10610200-10610800	ZNF genes & repeats	Primary T killer naive cells fromperipheralblood	blood
9	chr8:10610400-10610600	Bivalent Enhancer	Esophagus	oesophagus
10	chr8:10610400-10610600	ZNF genes & repeats	HepG2	liver
11	chr8:10610400-10614200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr8:10610600-10620400	Weak transcription	HepG2	liver
13	chr8:10610800-10622200	Weak transcription	Primary B cells from cord blood	blood
14	chr8:10610800-10662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
15	chr8:10611200-10624400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr8:10612600-10612800	Weak transcription	Pancreas	Pancrea
17	chr8:10612600-10617600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr8:10612600-10621600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:10612800-10621600	Weak transcription	Spleen	Spleen
20	chr8:10613200-10613400	ZNF genes & repeats	Aorta	Aorta
21	chr8:10613200-10622600	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr8:10613400-10621600	Weak transcription	Aorta	Aorta
23	chr8:10613600-10614800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:10613600-10614800	Enhancers	HMEC	breast
25	chr8:10613600-10618400	Weak transcription	Skeletal Muscle Female	skeletal muscle
26	chr8:10613600-10618800	Weak transcription	Fetal Muscle Leg	muscle
27	chr8:10613800-10617800	Weak transcription	Ovary	ovary
28	chr8:10614000-10614800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr8:10614000-10614800	Enhancers	Esophagus	oesophagus
30	chr8:10614000-10614800	Enhancers	Placenta	Placenta
31	chr8:10614200-10614400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr8:10614200-10614800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr8:10614200-10614800	Enhancers	Hela-S3	cervix
35	chr8:10614200-10614800	Enhancers	NHEK	skin
36	chr8:10614200-10616600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr8:10614200-10621400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
38	chr8:10614400-10614800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr8:10614400-10634200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr8:10614600-10616600	Weak transcription	K562	blood
41	chr8:10614800-10616000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr8:10614800-10616800	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr8:10614800-10617200	Weak transcription	Esophagus	oesophagus
44	chr8:10614800-10617400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr8:10614800-10617600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr8:10614800-10617600	Weak transcription	HMEC	breast
47	chr8:10614800-10617600	Weak transcription	NHEK	skin
48	chr8:10614800-10617800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr8:10614800-10618400	Weak transcription	Placenta	Placenta
50	chr8:10614800-10618600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

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