Variant report

Variant	nsv887435
Chromosome Location	chr7:6613604-6713985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3889)
CpG islands
(count:4825)
Chromatin interactive
region (count:193)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3889 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6618130-6618589	HepG2	liver:	n/a	n/a
2	ARID3A	chr7:6614192-6614418	HepG2	liver:	n/a	n/a
3	ARID3A	chr7:6629531-6629849	HepG2	liver:	n/a	n/a
4	ARID3A	chr7:6615037-6615691	HepG2	liver:	n/a	n/a
5	ARID3A	chr7:6629468-6629712	K562	blood:	n/a	n/a
6	ARID3A	chr7:6618274-6618393	K562	blood:	n/a	n/a
7	ARID3A	chr7:6614150-6614475	K562	blood:	n/a	n/a
8	ARID3A	chr7:6616934-6617136	K562	blood:	n/a	n/a
9	ARID3A	chr7:6616649-6617363	HepG2	liver:	n/a	n/a
10	ARID3A	chr7:6680032-6680221	K562	blood:	n/a	n/a
11	ATF1	chr7:6616890-6617293	K562	blood:	n/a	n/a
12	ATF1	chr7:6652571-6652812	K562	blood:	n/a	n/a
13	ATF1	chr7:6618390-6618532	K562	blood:	n/a	n/a
14	ATF2	chr7:6616855-6617276	GM12878	blood:	n/a	n/a
15	ATF2	chr7:6676670-6676974	GM12878	blood:	n/a	n/a
16	ATF2	chr7:6616856-6617355	GM12878	blood:	n/a	n/a
17	ATF2	chr7:6629394-6629712	GM12878	blood:	n/a	n/a
18	ATF2	chr7:6616962-6617218	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF2	chr7:6616892-6617306	H1-hESC	embryonic stem cell:	n/a	n/a
20	ATF3	chr7:6676764-6677038	K562	blood:	n/a	n/a
21	ATF3	chr7:6629337-6629771	A549	lung:	n/a	chr7:6629523-6629532 chr7:6629564-6629584
22	ATF3	chr7:6676663-6677108	GM12878	blood:	n/a	n/a
23	ATF3	chr7:6629344-6630003	A549	lung:	n/a	chr7:6629523-6629532 chr7:6629564-6629584
24	ATF3	chr7:6616918-6617188	K562	blood:	n/a	n/a
25	ATF3	chr7:6676729-6677016	HepG2	liver:	n/a	n/a
26	ATF3	chr7:6679904-6680092	K562	blood:	n/a	n/a
27	ATF3	chr7:6616841-6617244	K562	blood:	n/a	n/a
28	ATF3	chr7:6676775-6677020	GM12878	blood:	n/a	n/a
29	BACH1	chr7:6677373-6677430	K562	blood:	n/a	n/a
30	BACH1	chr7:6617014-6617175	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr7:6676413-6677735	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr7:6703886-6703996	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr7:6676690-6676978	K562	blood:	n/a	n/a
34	BACH1	chr7:6630335-6630344	K562	blood:	n/a	n/a
35	BACH1	chr7:6629362-6630071	H1-hESC	embryonic stem cell:	n/a	n/a
36	BATF	chr7:6659295-6659530	GM12878	blood:	n/a	n/a
37	BATF	chr7:6679547-6679737	GM12878	blood:	n/a	n/a
38	BCL11A	chr7:6616917-6617253	GM12878	blood:	n/a	chr7:6617026-6617035
39	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
40	BCL3	chr7:6616889-6617225	GM12878	blood:	n/a	chr7:6617026-6617035
41	BCL3	chr7:6629362-6630010	GM12878	blood:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629775-6629788 chr7:6629561-6629574 chr7:6629733-6629746 chr7:6629799-6629812
42	BCL3	chr7:6662021-6662558	GM12878	blood:	n/a	chr7:6662039-6662052 chr7:6662045-6662058 chr7:6662050-6662059 chr7:6662047-6662056 chr7:6662040-6662053 chr7:6662044-6662053 chr7:6662036-6662049
43	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
44	BCL3	chr7:6662073-6662402	GM12878	blood:	n/a	n/a
45	BCL3	chr7:6629789-6630335	A549	lung:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629799-6629812
46	BCL3	chr7:6676620-6677051	GM12878	blood:	n/a	chr7:6676897-6676906
47	BCLAF1	chr7:6616883-6617349	GM12878	blood:	n/a	chr7:6617026-6617035
48	BCLAF1	chr7:6641859-6642232	GM12878	blood:	n/a	n/a
49	BCLAF1	chr7:6616882-6617340	GM12878	blood:	n/a	chr7:6617026-6617035
50	BCLAF1	chr7:6629326-6630156	GM12878	blood:	n/a	chr7:6629794-6629807 chr7:6629869-6629878 chr7:6629872-6629881 chr7:6629775-6629788 chr7:6629561-6629574 chr7:6629733-6629746 chr7:6629799-6629812

(count:4825 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6666368-6666418	Hepatocyte	liver:	n/a
2	chr7:6629350-6629400	SKMC	muscle:	n/a
3	chr7:6677265-6677315	HAEpiC	amniotic membrane:	n/a
4	chr7:6617264-6617314	SK-N-SH_RA	brain:	n/a
5	chr7:6689218-6689268	A549	lung:	n/a
6	chr7:6693334-6693384	IMR90	lung:	fetal
7	chr7:6666368-6666418	Hepatocyte	liver:	n/a
8	chr7:6629350-6629400	SKMC	muscle:	n/a
9	chr7:6677265-6677315	HAEpiC	amniotic membrane:	n/a
10	chr7:6617264-6617314	SK-N-SH_RA	brain:	n/a
11	chr7:6689218-6689268	A549	lung:	n/a
12	chr7:6693334-6693384	IMR90	lung:	fetal
13	chr7:6655973-6656023	Hepatocyte	liver:	n/a
14	chr7:6703533-6703583	NB4	blood:	n/a
15	chr7:6698992-6699042	A549	lung:	n/a
16	chr7:6681379-6681429	GM19239	blood:	n/a
17	chr7:6681379-6681429	NHBE	bronchial:	n/a
18	chr7:6616423-6616473	GM19239	blood:	n/a
19	chr7:6699526-6699576	GM19239	blood:	n/a
20	chr7:6704194-6704244	CMK	blood:	n/a
21	chr7:6680085-6680135	HRPEpiC	eye:	n/a
22	chr7:6676001-6676051	NB4	blood:	n/a
23	chr7:6648166-6648216	NHDF-neo	bronchial:	n/a
24	chr7:6631520-6631570	Jurkat	blood:	n/a
25	chr7:6629806-6629856	CMK	blood:	n/a
26	chr7:6655711-6655761	AG09309	skin:	n/a
27	chr7:6676630-6676680	ProgFib	skin:	n/a
28	chr7:6696120-6696170	A549	lung:	n/a
29	chr7:6631520-6631570	K562	blood:	n/a
30	chr7:6655727-6655777	LNCaP	prostate:	n/a
31	chr7:6690313-6690363	SK-N-SH	brain:	n/a
32	chr7:6676001-6676051	AG09319	gingival:	n/a
33	chr7:6694978-6695028	HCM	heart:	n/a
34	chr7:6676630-6676680	RPTEC	kidney:	n/a
35	chr7:6617294-6617344	ProgFib	skin:	n/a
36	chr7:6647955-6648005	T-47D	breast:	n/a
37	chr7:6654422-6654472	AG09309	skin:	n/a
38	chr7:6614945-6614995	HCF	heart:	n/a
39	chr7:6676832-6676882	HRCEpiC	kidney:	n/a
40	chr7:6694978-6695028	MCF-7	breast:	n/a
41	chr7:6617276-6617326	RPTEC	kidney:	n/a
42	chr7:6693334-6693384	NHBE	bronchial:	n/a
43	chr7:6647955-6648005	HEEpiC	esophagus:	n/a
44	chr7:6676168-6676218	NB4	blood:	n/a
45	chr7:6694373-6694423	CMK	blood:	n/a
46	chr7:6647235-6647285	HNPCEpiC	eye:	n/a
47	chr7:6629515-6629565	K562	blood:	n/a
48	chr7:6655973-6656023	GM19239	blood:	n/a
49	chr7:6655711-6655761	BE2_C	brain:	n/a
50	chr7:6617294-6617344	AG04450	lung:	fetal

(count:193 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
2	chr7:6632840..6635572-chr7:6638804..6641530,2	K562	blood:
3	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
4	chr13:41837354..41837965-chr7:6616517..6617122,2	NB4	blood:
5	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:
6	chr7:6676193..6679067-chr7:6744810..6746794,4	K562	blood:
7	chr7:6641830..6642345-chr7:6698974..6699620,2	MCF-7	breast:
8	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
9	chr7:6614289..6616112-chr7:6628784..6631190,2	K562	blood:
10	chr7:6656839..6659879-chr7:6661538..6663786,3	K562	blood:
11	chr7:6628470..6631345-chr7:6645774..6647666,2	MCF-7	breast:
12	chr7:6641654..6643210-chr7:6674814..6676517,2	MCF-7	breast:
13	chr7:6628057..6630995-chr7:6646189..6648379,2	K562	blood:
14	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
15	chr7:6642714..6644762-chr7:6645777..6647383,2	K562	blood:
16	chr7:6645338..6648088-chr7:6676638..6679438,2	MCF-7	breast:
17	chr7:6696313..6698315-chr7:6745284..6746997,2	K562	blood:
18	chr7:6621445..6626175-chr7:6626576..6631235,7	MCF-7	breast:
19	chr7:6637338..6640081-chr7:6675258..6678566,5	MCF-7	breast:
20	chr7:6619535..6621612-chr7:6623475..6625158,2	MCF-7	breast:
21	chr7:6666562..6671587-chr7:6674314..6680724,9	MCF-7	breast:
22	chr7:6655297..6658106-chr7:6659491..6662615,3	K562	blood:
23	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:
24	chr7:6640896..6642429-chr7:6654051..6656617,2	MCF-7	breast:
25	chr7:6570467..6572933-chr7:6675256..6676794,2	MCF-7	breast:
26	chr7:6628238..6630542-chr7:6653702..6656593,2	MCF-7	breast:
27	chr7:6617184..6619983-chr7:6640766..6643695,2	MCF-7	breast:
28	chr7:6564171..6565673-chr7:6642376..6644316,2	K562	blood:
29	chr7:6615687..6618664-chr7:6627812..6632591,8	MCF-7	breast:
30	chr7:6627960..6631587-chr7:6636185..6643600,9	MCF-7	breast:
31	chr7:6628303..6631132-chr7:6637511..6639950,2	K562	blood:
32	chr7:6614342..6622557-chr7:6625132..6631922,18	K562	blood:
33	chr7:6645718..6648142-chr7:6667020..6668593,2	K562	blood:
34	chr7:6614342..6622557-chr7:6625132..6631922,18	K562	blood:
35	chr7:6541950..6543739-chr7:6677071..6679453,2	K562	blood:
36	chr7:6641239..6643457-chr7:6645179..6647378,2	MCF-7	breast:
37	chr7:6619810..6621522-chr7:6637808..6639394,2	MCF-7	breast:
38	chr7:6616780..6617546-chr8:33370685..33371254,2	Hela-S3	cervix:
39	chr7:6692466..6696366-chr7:6696714..6698992,3	MCF-7	breast:
40	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
41	chr7:6523333..6525416-chr7:6628158..6630053,2	K562	blood:
42	chr7:6628608..6631556-chr7:6632692..6634274,2	K562	blood:
43	chr7:6642714..6644762-chr7:6645777..6647383,2	K562	blood:
44	chr7:6706877..6708740-chr7:6715302..6717943,2	K562	blood:
45	chr7:6631417..6634053-chr7:6644555..6647316,2	K562	blood:
46	chr7:6615703..6619364-chr7:6676501..6679314,4	K562	blood:
47	chr7:6536495..6538201-chr7:6614810..6616911,2	K562	blood:
48	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
49	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
50	chr7:6522590..6525464-chr7:6629667..6631342,2	K562	blood:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
2	lnc-AC073343.1-1	chr7:6704675-6704739	NONHSAT119055
3	lnc-AC073343.1-1	chr7:6704675-6705152	ENSG00000228010.1
4	lnc-C7orf26-1	chr7:6627278-6627705	NONHSAT119009
5	lnc-ZNF853-2	chr7:6679361-6680635	ucscGeneNc_uc003sqr_1
6	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119056
7	lnc-C7orf26-1	chr7:6623346-6623463	NONHSAT119009
8	lnc-GRID2IP-1	chr7:6628326-6628605	ENSG00000232581.1
9	lnc-AC073343.1-1	chr7:6703605-6703674	NONHSAT119055
10	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
11	lnc-AC073343.1-1	chr7:6712836-6714110	NONHSAT119055
12	lnc-GRID2IP-1	chr7:6627741-6628856	NONHSAT119018
13	lnc-AC073343.1-1	chr7:6704675-6704739	ENSG00000228010.1
14	lnc-AC073343.1-1	chr7:6712836-6713232	ENSG00000228010.1
15	lnc-AC073343.1-1	chr7:6704675-6704739	ENSG00000228010.1
16	lnc-AC073343.1-1	chr7:6704675-6705152	NONHSAT119056
17	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1
18	lnc-C7orf26-1	chr7:6621773-6622342	NONHSAT119009
19	lnc-AC073343.1-1	chr7:6703605-6703674	ENSG00000228010.1
20	lnc-AC073343.1-1	chr7:6712836-6713398	NONHSAT119056
21	lnc-ZNF853-2	chr7:6670130-6670199	ucscGeneNc_uc003sqr_1
22	lnc-GRID2IP-1	chr7:6628988-6629569	NONHSAT119018
23	lnc-GRID2IP-1	chr7:6618196-6618272	ENSG00000232581.1
24	lnc-GRID2IP-2	chr7:6616302-6616419	NONHSAT119002
25	lnc-ZNF12-1	chr7:6708412-6708689	expReg_chr7_763_-
26	lnc-GRID2IP-2	chr7:6616573-6616698	NONHSAT119002
27	lnc-ZNF853-2	chr7:6671200-6671264	ucscGeneNc_uc003sqr_1

No data

Variant related genes	Relation type
C7orf26	TF binding region
ENSG00000232581	TF binding region
ZNF316	TF binding region
ENSG00000260054	TF binding region
ENSG00000228010	TF binding region
ZNF853	TF binding region
ENSG00000198580	TF binding region
ZDHHC4	TF binding region
C7orf26	CpG island
ENSG00000232581	CpG island
ZNF316	CpG island
ENSG00000260054	CpG island
ENSG00000228010	CpG island
ZNF853	CpG island
ENSG00000198580	CpG island
ZDHHC4	CpG island
ENSG00000188825	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000259006	chromatin interactions
ENSG00000215045	chromatin interactions
ENSG00000133466	chromatin interactions
ENSG00000265692	chromatin interactions
ENSG00000242110	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000120662	chromatin interactions
ENSG00000157450	chromatin interactions
ENSG00000129696	chromatin interactions
ENSG00000077150	chromatin interactions
ENSG00000214194	chromatin interactions
ENSG00000239039	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000164535	chromatin interactions
ENSG00000265245	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000269781	chromatin interactions
ENSG00000228010	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000236609	chromatin interactions
ENSG00000136240	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000096384	chromatin interactions
ENSG00000110080	chromatin interactions
ENSG00000011260	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000074603	chromatin interactions
ENSG00000198580	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000164631	chromatin interactions

Extended variants
information (count: 5071 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:5071 , 50 per page) page: 1 2 3 4 5 6 7 ... 102

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7800401	chr7:6613604-6613605	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs62441297	chr7:6613624-6613625	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs191364331	chr7:6613672-6613673	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs377007531	chr7:6613716-6613717	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs115804494	chr7:6613721-6613722	Weak transcription Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs10260072	chr7:6613801-6613802	Weak transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs535857007	chr7:6613823-6613824	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554518857	chr7:6613825-6613826	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs562666577	chr7:6613831-6613832	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs533259630	chr7:6613848-6613849	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs369233003	chr7:6613902-6613903	Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs116208555	chr7:6614001-6614002	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs558700376	chr7:6614055-6614056	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs183077289	chr7:6614064-6614065	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs543869999	chr7:6614071-6614072	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs562253143	chr7:6614086-6614087	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs529597735	chr7:6614104-6614105	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs538497412	chr7:6614110-6614111	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs541806720	chr7:6614118-6614119	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs559935747	chr7:6614153-6614154	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs57032699	chr7:6614160-6614161	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs57565590	chr7:6614162-6614163	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs28676445	chr7:6614202-6614203	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs371432540	chr7:6614203-6614204	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs367888873	chr7:6614204-6614205	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs552625130	chr7:6614206-6614207	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs376197139	chr7:6614215-6614216	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs368577827	chr7:6614216-6614217	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs571032656	chr7:6614223-6614224	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs550449909	chr7:6614237-6614238	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs185995907	chr7:6614252-6614253	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs17199024	chr7:6614298-6614299	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190656486	chr7:6614332-6614333	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs113293806	chr7:6614453-6614454	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs200787115	chr7:6614502-6614503	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs183254551	chr7:6614507-6614508	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs371720460	chr7:6614512-6614513	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs376638846	chr7:6614522-6614523	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs78446493	chr7:6614524-6614525	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs201944949	chr7:6614526-6614527	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs397725929	chr7:6614537-6614538	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs149388754	chr7:6614538-6614539	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs565973043	chr7:6614606-6614607	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs4724824	chr7:6614662-6614663	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs57806682	chr7:6614666-6614667	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs4724825	chr7:6614668-6614669	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs534071256	chr7:6614693-6614694	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs558447469	chr7:6614720-6614721	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs187850261	chr7:6614780-6614781	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs193145461	chr7:6614785-6614786	Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:4544 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6578600-6616200	Weak transcription	Right Atrium	heart
2	chr7:6610400-6615800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr7:6611400-6615800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:6611400-6616600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:6611600-6615000	Weak transcription	Ovary	ovary
6	chr7:6611600-6615600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr7:6611600-6615800	Weak transcription	Hela-S3	cervix
8	chr7:6611600-6616000	Weak transcription	GM12878-XiMat	blood
9	chr7:6612200-6616200	Weak transcription	Fetal Muscle Trunk	muscle
10	chr7:6612600-6614000	Genic enhancers	HepG2	liver
11	chr7:6614000-6614400	Enhancers	HSMMtube	muscle
12	chr7:6614000-6614800	Enhancers	HepG2	liver
13	chr7:6614400-6616400	Weak transcription	HSMMtube	muscle
14	chr7:6614600-6614800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:6614800-6615200	Flanking Active TSS	HepG2	liver
16	chr7:6614800-6615800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr7:6615000-6615200	Enhancers	Ovary	ovary
18	chr7:6615000-6615200	Enhancers	A549	lung
19	chr7:6615200-6615400	Enhancers	HepG2	liver
20	chr7:6615200-6615800	Weak transcription	A549	lung
21	chr7:6615200-6616200	Weak transcription	Ovary	ovary
22	chr7:6615400-6616400	Flanking Active TSS	HepG2	liver
23	chr7:6615600-6615800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:6615600-6615800	Enhancers	Dnd41	blood
25	chr7:6615600-6615800	Active TSS	K562	blood
26	chr7:6615600-6616200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr7:6615600-6616200	Enhancers	NHDF-Ad	bronchial
28	chr7:6615800-6616000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:6615800-6616000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr7:6615800-6616000	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
31	chr7:6615800-6616000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
32	chr7:6615800-6616000	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:6615800-6616000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr7:6615800-6616000	Enhancers	Brain Angular Gyrus	brain
35	chr7:6615800-6616000	Enhancers	Brain Anterior Caudate	brain
36	chr7:6615800-6616000	Enhancers	Brain Hippocampus Middle	brain
37	chr7:6615800-6616000	Enhancers	Brain Inferior Temporal Lobe	brain
38	chr7:6615800-6616000	Enhancers	Fetal Lung	lung
39	chr7:6615800-6616000	Enhancers	A549	lung
40	chr7:6615800-6616200	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr7:6615800-6616200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr7:6615800-6616200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr7:6615800-6616200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr7:6615800-6616200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr7:6615800-6616200	Enhancers	Spleen	Spleen
46	chr7:6615800-6616400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr7:6615800-6616400	Enhancers	Primary hematopoietic stem cells	blood
48	chr7:6615800-6616400	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr7:6615800-6616400	Enhancers	Fetal Muscle Leg	muscle
50	chr7:6615800-6616400	Enhancers	Pancreas	Pancrea

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