Variant report

Variant	esv1830357
Chromosome Location	chr7:99562984-99617852
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2309)
CpG islands
(count:2201)
Chromatin interactive
region (count:120)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2309 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:99610285-99610671	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:99601325-99601936	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:99614020-99614567	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:99612999-99613317	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:99577288-99577300	K562	blood:	n/a	n/a
6	ARID3A	chr7:99588561-99588855	K562	blood:	n/a	n/a
7	ARID3A	chr7:99595227-99595537	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:99591808-99592148	HepG2	liver:	n/a	n/a
9	ARID3A	chr7:99591850-99592144	K562	blood:	n/a	n/a
10	ARID3A	chr7:99613002-99613272	K562	blood:	n/a	n/a
11	ARID3A	chr7:99573511-99574236	HepG2	liver:	n/a	n/a
12	ARID3A	chr7:99588540-99588839	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:99578392-99578401	HepG2	liver:	n/a	n/a
14	ATF1	chr7:99613008-99613355	K562	blood:	n/a	n/a
15	ATF2	chr7:99595114-99595627	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr7:99595132-99595501	H1-hESC	embryonic stem cell:	n/a	n/a
17	ATF2	chr7:99612925-99613402	GM12878	blood:	n/a	n/a
18	ATF2	chr7:99588414-99588699	GM12878	blood:	n/a	n/a
19	ATF2	chr7:99612922-99613352	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF2	chr7:99588383-99588853	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr7:99612906-99613380	A549	lung:	n/a	n/a
22	ATF3	chr7:99588519-99588908	A549	lung:	n/a	n/a
23	ATF3	chr7:99612938-99613479	K562	blood:	n/a	n/a
24	BACH1	chr7:99588600-99588743	K562	blood:	n/a	n/a
25	BACH1	chr7:99612991-99613276	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr7:99612974-99613349	GM12878	blood:	n/a	n/a
27	BCL3	chr7:99612971-99613328	GM12878	blood:	n/a	chr7:99613205-99613214
28	BCL3	chr7:99612943-99613384	A549	lung:	n/a	chr7:99613205-99613214
29	BCLAF1	chr7:99612895-99613380	GM12878	blood:	n/a	chr7:99613205-99613214
30	BCLAF1	chr7:99595032-99595589	GM12878	blood:	n/a	chr7:99595317-99595326
31	BCLAF1	chr7:99612943-99613345	GM12878	blood:	n/a	chr7:99613205-99613214
32	BHLHE40	chr7:99595201-99595644	HepG2	liver:	n/a	n/a
33	BHLHE40	chr7:99612987-99613358	K562	blood:	n/a	n/a
34	BHLHE40	chr7:99601366-99601918	HepG2	liver:	n/a	n/a
35	BHLHE40	chr7:99577501-99577734	GM12878	blood:	n/a	n/a
36	BHLHE40	chr7:99577510-99577734	K562	blood:	n/a	n/a
37	BHLHE40	chr7:99588564-99588813	K562	blood:	n/a	n/a
38	BHLHE40	chr7:99576876-99576892	K562	blood:	n/a	n/a
39	BHLHE40	chr7:99595199-99595648	GM12878	blood:	n/a	n/a
40	BHLHE40	chr7:99573751-99574031	HepG2	liver:	n/a	n/a
41	BHLHE40	chr7:99591934-99592020	K562	blood:	n/a	n/a
42	BRCA1	chr7:99612967-99613336	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr7:99601493-99601826	HepG2	liver:	n/a	n/a
44	BRCA1	chr7:99591862-99592076	Hela-S3	cervix:	n/a	n/a
45	CBX3	chr7:99580102-99580449	K562	blood:	n/a	n/a
46	CBX3	chr7:99612953-99613313	K562	blood:	n/a	n/a
47	CBX3	chr7:99612836-99613459	K562	blood:	n/a	n/a
48	CBX3	chr7:99588497-99588920	K562	blood:	n/a	n/a
49	CBX3	chr7:99588462-99588995	K562	blood:	n/a	n/a
50	CCNT2	chr7:99613083-99613301	K562	blood:	n/a	n/a

(count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:99576539-99576589	MCF10A-Er-Src	breast:	n/a
2	chr7:99613147-99613197	HRE	kidney:	n/a
3	chr7:99613205-99613255	PANC-1	pancreas:	n/a
4	chr7:99564474-99564524	HUVEC	blood vessel:	n/a
5	chr7:99612773-99612823	HNPCEpiC	eye:	n/a
6	chr7:99576539-99576589	MCF10A-Er-Src	breast:	n/a
7	chr7:99613147-99613197	HRE	kidney:	n/a
8	chr7:99613205-99613255	PANC-1	pancreas:	n/a
9	chr7:99564474-99564524	HUVEC	blood vessel:	n/a
10	chr7:99612773-99612823	HNPCEpiC	eye:	n/a
11	chr7:99598775-99598825	GM19239	blood:	n/a
12	chr7:99573278-99573328	Caco-2	colon:	n/a
13	chr7:99613244-99613294	HCM	heart:	n/a
14	chr7:99574420-99574470	HCM	heart:	n/a
15	chr7:99564474-99564524	AG09309	skin:	n/a
16	chr7:99591962-99592012	HIPEpiC	eye:	n/a
17	chr7:99595658-99595708	AG10803	skin:	n/a
18	chr7:99588273-99588323	NH-A	brain:	n/a
19	chr7:99573278-99573328	K562	blood:	n/a
20	chr7:99613105-99613155	LNCaP	prostate:	n/a
21	chr7:99574420-99574470	HCT-116	colon:	n/a
22	chr7:99574420-99574470	GM19239	blood:	n/a
23	chr7:99613185-99613235	NHBE	bronchial:	n/a
24	chr7:99612634-99612684	GM12892	blood:	n/a
25	chr7:99598775-99598825	SKMC	muscle:	n/a
26	chr7:99564474-99564524	SK-N-SH_RA	brain:	n/a
27	chr7:99613205-99613255	PFSK-1	brain:	n/a
28	chr7:99613244-99613294	HL-60	blood:	n/a
29	chr7:99564474-99564524	AG09319	gingival:	n/a
30	chr7:99588561-99588611	HCT-116	colon:	n/a
31	chr7:99588657-99588707	NT2-D1	testis:	n/a
32	chr7:99576547-99576597	Hela-S3	cervix:	n/a
33	chr7:99613205-99613255	Jurkat	blood:	n/a
34	chr7:99613205-99613255	NHDF-neo	bronchial:	n/a
35	chr7:99588335-99588385	RPTEC	kidney:	n/a
36	chr7:99613105-99613155	GM12891	blood:	n/a
37	chr7:99587136-99587186	NT2-D1	testis:	n/a
38	chr7:99576539-99576589	HIPEpiC	eye:	n/a
39	chr7:99588335-99588385	NH-A	brain:	n/a
40	chr7:99613105-99613155	AG10803	skin:	n/a
41	chr7:99598775-99598825	Caco-2	colon:	n/a
42	chr7:99614209-99614259	BE2_C	brain:	n/a
43	chr7:99595276-99595326	HEK293	kidney:	embryo
44	chr7:99595095-99595145	PrEC	prostate:	n/a
45	chr7:99612634-99612684	SKMC	muscle:	n/a
46	chr7:99591962-99592012	LNCaP	prostate:	n/a
47	chr7:99595348-99595398	NHBE	bronchial:	n/a
48	chr7:99613147-99613197	MCF-7	breast:	n/a
49	chr7:99609831-99609881	LNCaP	prostate:	n/a
50	chr7:99595437-99595487	HRPEpiC	eye:	n/a

(count:120 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr7:99611801..99614602-chr7:99679230..99681000,2	MCF-7	breast:
2	chr7:99612390..99616211-chr7:99697108..99699457,4	K562	blood:
3	chr7:99614250..99615860-chr7:99701481..99703800,2	K562	blood:
4	chr7:99510202..99510941-chr7:99588109..99589102,2	MCF-7	breast:
5	chr7:99604525..99607316-chr7:99612606..99614648,4	MCF-7	breast:
6	chr7:99591491..99592473-chr7:99650892..99651464,2	K562	blood:
7	chr7:99510483..99511406-chr7:99588237..99589135,5	MCF-7	breast:
8	chr7:99612131..99615242-chr7:99723277..99726662,3	K562	blood:
9	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
10	chr7:99601762..99603433-chr7:99603449..99606278,2	K562	blood:
11	chr7:99609554..99611376-chr7:99679608..99681237,2	K562	blood:
12	chr7:99510472..99511406-chr7:99588187..99589134,5	K562	blood:
13	chr7:99580447..99583544-chr7:99586500..99589317,4	K562	blood:
14	chr7:99591418..99594065-chr7:99611454..99615168,4	MCF-7	breast:
15	chr7:99513401..99515939-chr7:99585193..99587203,2	K562	blood:
16	chr7:99590363..99592421-chr7:99597136..99600060,2	MCF-7	breast:
17	chr7:99592003..99594227-chr7:99676787..99679509,2	K562	blood:
18	chr7:99214190..99217311-chr7:99612118..99614634,3	K562	blood:
19	chr7:99588651..99591308-chr7:99612703..99615208,2	K562	blood:
20	chr7:99601553..99605102-chr7:99669434..99672992,3	K562	blood:
21	chr7:99588651..99591308-chr7:99612703..99615208,2	K562	blood:
22	chr7:99587817..99590250-chr7:99755042..99756960,2	K562	blood:
23	chr7:99515843..99517674-chr7:99586833..99588501,2	MCF-7	breast:
24	chr7:99589288..99591810-chr7:99612834..99614804,4	MCF-7	breast:
25	chr19:55918691..55919435-chr7:99612825..99613381,2	HCT-116	colon:
26	chr7:99590918..99594546-chr7:99596737..99599787,3	K562	blood:
27	chr7:99577230..99578015-chr7:99588605..99589135,2	MCF-7	breast:
28	chr7:99591337..99592929-chr7:99646894..99648865,2	MCF-7	breast:
29	chr7:99591865..99592813-chr7:99679412..99679994,2	K562	blood:
30	chr7:99588733..99590753-chr7:99595568..99598472,2	K562	blood:
31	chr7:99580447..99585207-chr7:99587129..99590928,6	K562	blood:
32	chr7:99576315..99578805-chr7:99697574..99699659,2	MCF-7	breast:
33	chr7:99588477..99590075-chr7:99697467..99699544,2	K562	blood:
34	chr7:99552086..99554197-chr7:99560760..99564029,3	MCF-7	breast:
35	chr7:99601356..99603407-chr7:99644840..99648336,3	MCF-7	breast:
36	chr7:99612316..99614498-chr7:99678113..99681049,2	MCF-7	breast:
37	chr7:99616524..99619632-chr7:99677690..99679745,3	K562	blood:
38	chr1:45196470..45197118-chr7:99613158..99613683,2	Hela-S3	cervix:
39	chr7:99564809..99567213-chr7:99568029..99570135,2	K562	blood:
40	chr7:99611430..99615857-chr7:99675156..99681193,15	K562	blood:
41	chr7:99608355..99609979-chr7:99641023..99642646,2	MCF-7	breast:
42	chr7:99601499..99602018-chr7:99663035..99663790,2	MCF-7	breast:
43	chr7:99590918..99594546-chr7:99596737..99599787,3	K562	blood:
44	chr7:99598705..99603395-chr7:99611992..99615824,4	MCF-7	breast:
45	chr7:99577230..99578015-chr7:99588605..99589135,2	MCF-7	breast:
46	chr7:99577974..99580142-chr7:99679417..99681794,2	MCF-7	breast:
47	chr7:99600850..99603029-chr7:99645305..99648884,3	K562	blood:
48	chr10:43133589..43134241-chr7:99612910..99613726,2	NB4	blood:
49	chr7:99573022..99574848-chr7:99645324..99647689,2	K562	blood:
50	chr7:99524861..99526650-chr7:99605841..99607428,2	MCF-7	breast:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZKSCAN1-1	chr7:99608999-99609247	XLOC_006188
2	lnc-ZKSCAN1-1	chr7:99597006-99597115	XLOC_006188
3	lnc-ZKSCAN1-2	chr7:99587971-99588326	expReg_chr7_6373_+
4	lnc-ZKSCAN1-1	chr7:99597123-99597186	XLOC_006188
5	lnc-ZKSCAN1-1	chr7:99608999-99609239	XLOC_006188
6	lnc-ZKSCAN1-1	chr7:99608999-99609247	XLOC_006188
7	lnc-ZKSCAN1-1	chr7:99605931-99605945	XLOC_006188
8	lnc-ZKSCAN1-1	chr7:99608999-99609249	XLOC_006188
9	lnc-ZKSCAN1-1	chr7:99605669-99605945	XLOC_006188
10	lnc-ZKSCAN1-1	chr7:99606205-99606730	XLOC_006188
11	lnc-ZKSCAN1-1	chr7:99597002-99597115	XLOC_006188
12	lnc-ZKSCAN1-1	chr7:99594667-99594733	XLOC_006188
13	lnc-ZKSCAN1-1	chr7:99605744-99605862	XLOC_006188
14	lnc-ZKSCAN1-1	chr7:99595355-99595546	XLOC_006188

No data

Variant related genes	Relation type
ZKSCAN1	TF binding region
ENSG00000235713	TF binding region
AZGP1	TF binding region
AZGP1P1	TF binding region
ZKSCAN1	CpG island
ENSG00000235713	CpG island
AZGP1	CpG island
AZGP1P1	CpG island
ENSG00000221838	chromatin interactions
ENSG00000237640	chromatin interactions
ENSG00000235713	chromatin interactions
ENSG00000106261	chromatin interactions
ENSG00000197153	chromatin interactions
ENSG00000166529	chromatin interactions
ENSG00000146833	chromatin interactions
ENSG00000272888	chromatin interactions
ENSG00000108106	chromatin interactions
ENSG00000166997	chromatin interactions
ENSG00000214309	chromatin interactions
ENSG00000176402	chromatin interactions
ENSG00000106290	chromatin interactions
ENSG00000214252	chromatin interactions
ENSG00000196693	chromatin interactions
ENSG00000146826	chromatin interactions
ENSG00000197037	chromatin interactions
ENSG00000166526	chromatin interactions
ENSG00000235077	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000160862	chromatin interactions
ENSG00000168090	chromatin interactions
ENSG00000272373	chromatin interactions
ENSG00000166508	chromatin interactions
ENSG00000137154	chromatin interactions
ENSG00000242798	chromatin interactions
ENSG00000051108	chromatin interactions
NUP153	miRNA target sites
ASCC2	miRNA target sites
KCTD15	miRNA target sites
TMEM45A	miRNA target sites
BRD1	miRNA target sites
C11orf82	miRNA target sites
ARSJ	miRNA target sites

Extended variants
information (count: 2196 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:2196 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2107350	chr7:99562984-99562985	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570887926	chr7:99563010-99563011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs538281609	chr7:99563012-99563013	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs548273312	chr7:99563031-99563032	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs551448962	chr7:99563043-99563044	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs78419728	chr7:99563049-99563050	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs188204889	chr7:99563054-99563055	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs560254179	chr7:99563072-99563073	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs565684328	chr7:99563078-99563079	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536349601	chr7:99563088-99563089	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs554825026	chr7:99563130-99563131	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576727139	chr7:99563153-99563154	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs537713683	chr7:99563179-99563180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs559322601	chr7:99563198-99563199	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs376334853	chr7:99563201-99563202	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577297967	chr7:99563204-99563205	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs541109655	chr7:99563205-99563206	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181045303	chr7:99563211-99563212	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs571487551	chr7:99563244-99563245	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs375614769	chr7:99563246-99563247	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185561220	chr7:99563282-99563283	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs542322766	chr7:99563318-99563319	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190364205	chr7:99563363-99563364	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs183806387	chr7:99563376-99563377	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs200673745	chr7:99563399-99563400	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs142590385	chr7:99563411-99563412	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs187112997	chr7:99563421-99563422	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs150594272	chr7:99563437-99563438	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs527862156	chr7:99563493-99563494	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs551246592	chr7:99563515-99563516	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs532130535	chr7:99563532-99563533	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs552380343	chr7:99563556-99563557	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs76286169	chr7:99563571-99563572	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs565680950	chr7:99563590-99563591	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs538119360	chr7:99563619-99563620	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs535934129	chr7:99563665-99563666	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192495079	chr7:99563679-99563680	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570243221	chr7:99563707-99563708	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs550455959	chr7:99563711-99563712	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537680047	chr7:99563721-99563722	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371533729	chr7:99563814-99563815	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201247837	chr7:99563820-99563821	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs559286561	chr7:99563866-99563867	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs567914902	chr7:99563868-99563869	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs182533104	chr7:99563873-99563874	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs535333169	chr7:99563921-99563922	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs186632860	chr7:99563949-99563950	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112818296	chr7:99563950-99563951	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2527882	chr7:99563961-99563962	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs10235128	chr7:99563984-99563985	Strong transcription Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Prostate cancer	16461572	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Malignant melanoma	17260012	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Chronic myeloid leukemia	21384125	CNVD
Bladder cancer	21909424	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	16608533	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Liver carcinoma	19366792	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Adenocarcinoma	19607727	CNVD
Multiple myeloma	16461302	CNVD
Breast cancer	21858162	CNVD
Emphysema	19352772	CNVD
Effusion lymphoma	18079361	CNVD
Medulloblastoma	17653508	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Autism	19401682	CNVD
Neuroticism	17667963	CNVD
Breast cancer	21509527	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Prostate cancer	18632612	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1858 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:99553800-99563200	Weak transcription	Liver	Liver
2	chr7:99554000-99565000	Weak transcription	HepG2	liver
3	chr7:99561600-99564000	Weak transcription	Pancreas	Pancrea
4	chr7:99562600-99573000	Weak transcription	Left Ventricle	heart
5	chr7:99563200-99567000	Strong transcription	Liver	Liver
6	chr7:99563400-99572800	Weak transcription	Brain Substantia Nigra	brain
7	chr7:99563400-99573000	Weak transcription	Gastric	stomach
8	chr7:99564000-99565600	Strong transcription	Pancreas	Pancrea
9	chr7:99564600-99564800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr7:99564800-99567600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr7:99565000-99565800	Strong transcription	HepG2	liver
12	chr7:99565400-99571600	Weak transcription	Adipose Nuclei	Adipose
13	chr7:99565600-99567600	Weak transcription	Pancreas	Pancrea
14	chr7:99565800-99568200	Weak transcription	HepG2	liver
15	chr7:99566000-99572400	Weak transcription	Right Ventricle	heart
16	chr7:99566800-99567000	Enhancers	Lung	lung
17	chr7:99567000-99569000	Weak transcription	Lung	lung
18	chr7:99567000-99570600	Genic enhancers	Liver	Liver
19	chr7:99567600-99567800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr7:99567600-99567800	Enhancers	Pancreas	Pancrea
21	chr7:99567800-99568200	Weak transcription	Pancreas	Pancrea
22	chr7:99567800-99578000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr7:99568200-99569600	Strong transcription	HepG2	liver
24	chr7:99568200-99570000	Genic enhancers	Pancreas	Pancrea
25	chr7:99568400-99568800	Weak transcription	Brain Anterior Caudate	brain
26	chr7:99569000-99569600	Enhancers	Lung	lung
27	chr7:99569600-99571600	Weak transcription	HepG2	liver
28	chr7:99570000-99570400	Enhancers	Pancreas	Pancrea
29	chr7:99570400-99572600	Weak transcription	Pancreas	Pancrea
30	chr7:99570600-99570800	Enhancers	Liver	Liver
31	chr7:99570800-99571400	Flanking Active TSS	Liver	Liver
32	chr7:99571400-99573800	Active TSS	Liver	Liver
33	chr7:99571600-99571800	Enhancers	Adipose Nuclei	Adipose
34	chr7:99571600-99572400	Enhancers	HepG2	liver
35	chr7:99571800-99572400	Weak transcription	Adipose Nuclei	Adipose
36	chr7:99572400-99572600	Flanking Active TSS	Adipose Nuclei	Adipose
37	chr7:99572400-99572800	Flanking Active TSS	HepG2	liver
38	chr7:99572400-99573600	Active TSS	Pancreatic Islets	Pancreatic Islet
39	chr7:99572400-99573600	Active TSS	Right Ventricle	heart
40	chr7:99572600-99573400	Active TSS	Adipose Nuclei	Adipose
41	chr7:99572600-99573800	Active TSS	Pancreas	Pancrea
42	chr7:99572800-99573800	Active TSS	HepG2	liver
43	chr7:99572800-99574000	Active TSS	Brain Substantia Nigra	brain
44	chr7:99572800-99574200	Enhancers	Brain Cingulate Gyrus	brain
45	chr7:99573000-99573600	Active TSS	Duodenum Mucosa	Duodenum
46	chr7:99573000-99573600	Active TSS	Left Ventricle	heart
47	chr7:99573000-99573800	Active TSS	Gastric	stomach
48	chr7:99573000-99574200	Enhancers	Brain Inferior Temporal Lobe	brain
49	chr7:99573400-99573800	Flanking Active TSS	Adipose Nuclei	Adipose
50	chr7:99573400-99573800	Active TSS	Brain Anterior Caudate	brain

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