Variant report

Variant	nsv606007
Chromosome Location	chr7:6666501-6692407
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:978)
CpG islands
(count:978)
Chromatin interactive
region (count:63)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:6680032-6680221	K562	blood:	n/a	n/a
2	ATF2	chr7:6676670-6676974	GM12878	blood:	n/a	n/a
3	ATF3	chr7:6676729-6677016	HepG2	liver:	n/a	n/a
4	ATF3	chr7:6676663-6677108	GM12878	blood:	n/a	n/a
5	ATF3	chr7:6679904-6680092	K562	blood:	n/a	n/a
6	ATF3	chr7:6676775-6677020	GM12878	blood:	n/a	n/a
7	ATF3	chr7:6676764-6677038	K562	blood:	n/a	n/a
8	BACH1	chr7:6676413-6677735	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr7:6676690-6676978	K562	blood:	n/a	n/a
10	BACH1	chr7:6677373-6677430	K562	blood:	n/a	n/a
11	BATF	chr7:6679547-6679737	GM12878	blood:	n/a	n/a
12	BCL3	chr7:6676620-6677051	GM12878	blood:	n/a	chr7:6676897-6676906
13	BCLAF1	chr7:6676612-6677075	GM12878	blood:	n/a	chr7:6676897-6676906
14	BHLHE40	chr7:6685656-6685802	K562	blood:	n/a	n/a
15	BHLHE40	chr7:6676722-6677023	K562	blood:	n/a	n/a
16	BHLHE40	chr7:6676643-6677601	GM12878	blood:	n/a	chr7:6677407-6677423
17	BHLHE40	chr7:6677264-6677647	K562	blood:	n/a	chr7:6677407-6677423
18	BHLHE40	chr7:6679587-6679733	GM12878	blood:	n/a	n/a
19	BHLHE40	chr7:6679828-6680319	K562	blood:	n/a	n/a
20	BHLHE40	chr7:6676405-6676427	K562	blood:	n/a	n/a
21	CBX3	chr7:6676642-6676930	K562	blood:	n/a	n/a
22	CBX3	chr7:6677286-6677693	K562	blood:	n/a	n/a
23	CBX3	chr7:6679531-6680589	K562	blood:	n/a	n/a
24	CBX3	chr7:6679776-6680216	K562	blood:	n/a	n/a
25	CCNT2	chr7:6676308-6677623	K562	blood:	n/a	n/a
26	CEBPB	chr7:6679964-6680434	K562	blood:	n/a	n/a
27	CEBPB	chr7:6679421-6679645	A549	lung:	n/a	n/a
28	CEBPB	chr7:6679892-6680277	K562	blood:	n/a	n/a
29	CEBPB	chr7:6679380-6679580	HepG2	liver:	n/a	n/a
30	CEBPB	chr7:6679441-6679533	K562	blood:	n/a	n/a
31	CEBPD	chr7:6676694-6677135	HepG2	liver:	n/a	n/a
32	CEBPD	chr7:6676750-6677014	HepG2	liver:	n/a	n/a
33	CEBPD	chr7:6676684-6677078	K562	blood:	n/a	n/a
34	CHD1	chr7:6676646-6677040	GM12878	blood:	n/a	n/a
35	CHD1	chr7:6677295-6677418	GM12878	blood:	n/a	n/a
36	CHD1	chr7:6677773-6677776	GM12878	blood:	n/a	n/a
37	CHD2	chr7:6676748-6676948	Hela-S3	cervix:	n/a	n/a
38	CHD2	chr7:6680088-6680425	H1-hESC	embryonic stem cell:	n/a	n/a
39	CHD2	chr7:6676738-6677050	GM12878	blood:	n/a	n/a
40	CHD2	chr7:6677612-6677707	K562	blood:	n/a	n/a
41	CHD2	chr7:6677366-6677690	GM12878	blood:	n/a	n/a
42	CHD2	chr7:6679927-6680429	K562	blood:	n/a	n/a
43	CHD2	chr7:6676556-6676576	HepG2	liver:	n/a	n/a
44	CHD2	chr7:6688733-6688788	Hela-S3	cervix:	n/a	n/a
45	CREB1	chr7:6677194-6677588	A549	lung:	n/a	n/a
46	CREB1	chr7:6676488-6677125	HepG2	liver:	n/a	n/a
47	CREB1	chr7:6676419-6677071	A549	lung:	n/a	n/a
48	CREB1	chr7:6676811-6676987	A549	lung:	n/a	n/a
49	CTBP2	chr7:6677257-6677706	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr7:6677400-6677550	HFF-Myc	foreskin:	n/a	n/a

(count:978 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6676832-6676882	AG09319	gingival:	n/a
2	chr7:6689218-6689268	NHDF-neo	bronchial:	n/a
3	chr7:6676832-6676882	AG09319	gingival:	n/a
4	chr7:6689218-6689268	NHDF-neo	bronchial:	n/a
5	chr7:6677606-6677656	HCT-116	colon:	n/a
6	chr7:6677606-6677656	H1-hESC	embryonic stem cell:	embryo
7	chr7:6682784-6682834	IMR90	lung:	fetal
8	chr7:6689218-6689268	ovcar-3	ovarian:	n/a
9	chr7:6676832-6676882	HMEC	breast:	n/a
10	chr7:6676784-6676834	HAEpiC	amniotic membrane:	n/a
11	chr7:6674031-6674081	ovcar-3	ovarian:	n/a
12	chr7:6677606-6677656	HRPEpiC	eye:	n/a
13	chr7:6674031-6674081	BE2_C	brain:	n/a
14	chr7:6691949-6691999	ovcar-3	ovarian:	n/a
15	chr7:6677606-6677656	GM06990	blood:	n/a
16	chr7:6676168-6676218	HNPCEpiC	eye:	n/a
17	chr7:6681379-6681429	HIPEpiC	eye:	n/a
18	chr7:6676001-6676051	HRE	kidney:	n/a
19	chr7:6677265-6677315	IMR90	lung:	fetal
20	chr7:6690313-6690363	CMK	blood:	n/a
21	chr7:6676630-6676680	BE2_C	brain:	n/a
22	chr7:6682784-6682834	ECC-1	luminal epithelium:	n/a
23	chr7:6676168-6676218	AG04450	lung:	fetal
24	chr7:6680085-6680135	T-47D	breast:	n/a
25	chr7:6681379-6681429	NH-A	brain:	n/a
26	chr7:6677606-6677656	HL-60	blood:	n/a
27	chr7:6677433-6677483	ECC-1	luminal epithelium:	n/a
28	chr7:6676832-6676882	HRPEpiC	eye:	n/a
29	chr7:6677433-6677483	AG04449	skin:	fetal
30	chr7:6676630-6676680	SKMC	muscle:	n/a
31	chr7:6677433-6677483	IMR90	lung:	fetal
32	chr7:6677265-6677315	SK-N-SH	brain:	n/a
33	chr7:6676832-6676882	NT2-D1	testis:	n/a
34	chr7:6690313-6690363	PrEC	prostate:	n/a
35	chr7:6680085-6680135	HMEC	breast:	n/a
36	chr7:6676630-6676680	HL-60	blood:	n/a
37	chr7:6676832-6676882	HCPEpiC	choroid plexus:	n/a
38	chr7:6681379-6681429	SK-N-SH	brain:	n/a
39	chr7:6676168-6676218	NT2-D1	testis:	n/a
40	chr7:6681379-6681429	HRPEpiC	eye:	n/a
41	chr7:6676784-6676834	HUVEC	blood vessel:	n/a
42	chr7:6677606-6677656	Hela-S3	cervix:	n/a
43	chr7:6677433-6677483	HRPEpiC	eye:	n/a
44	chr7:6676784-6676834	K562	blood:	n/a
45	chr7:6677606-6677656	ECC-1	luminal epithelium:	n/a
46	chr7:6676784-6676834	AG09309	skin:	n/a
47	chr7:6691949-6691999	BE2_C	brain:	n/a
48	chr7:6676001-6676051	PFSK-1	brain:	n/a
49	chr7:6682784-6682834	PANC-1	pancreas:	n/a
50	chr7:6676832-6676882	H1-hESC	embryonic stem cell:	embryo

(count:63 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:6637338..6640081-chr7:6675258..6678566,5	MCF-7	breast:
2	chr7:6521808..6524278-chr7:6666674..6668575,2	K562	blood:
3	chr7:6660564..6662217-chr7:6683757..6686361,2	MCF-7	breast:
4	chr7:6641654..6643210-chr7:6674814..6676517,2	MCF-7	breast:
5	chr7:6650218..6651893-chr7:6687593..6690254,2	K562	blood:
6	chr7:6683480..6686518-chr7:6689197..6691289,3	MCF-7	breast:
7	chr7:6672567..6674181-chr7:6688854..6690680,2	K562	blood:
8	chr7:6668744..6673941-chr7:6674951..6679228,16	MCF-7	breast:
9	chr7:6628215..6631115-chr7:6675239..6679126,9	MCF-7	breast:
10	chr7:6659549..6661363-chr7:6670073..6672008,2	K562	blood:
11	chr7:6522385..6525546-chr7:6675389..6679461,5	MCF-7	breast:
12	chr7:6675427..6681659-chr7:6684293..6688490,10	MCF-7	breast:
13	chr7:6688371..6689911-chr7:6696909..6698726,2	K562	blood:
14	chr7:6645718..6648142-chr7:6667020..6668593,2	K562	blood:
15	chr7:6627001..6634994-chr7:6673643..6681623,15	MCF-7	breast:
16	chr7:6674043..6676883-chr7:6677067..6680291,5	K562	blood:
17	chr7:6668677..6671566-chr7:6683216..6685538,2	MCF-7	breast:
18	chr10:104155341..104155841-chr7:6676464..6677005,2	Hela-S3	cervix:
19	chr7:6629079..6630175-chr7:6676992..6678000,4	MCF-7	breast:
20	chr7:6626891..6631454-chr7:6676260..6679154,6	K562	blood:
21	chr7:6654514..6658630-chr7:6675114..6678876,5	MCF-7	breast:
22	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
23	chr7:6685863..6688294-chr7:6688920..6690681,2	MCF-7	breast:
24	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
25	chr12:56510812..56512603-chr7:6677169..6678802,2	MCF-7	breast:
26	chr7:6626891..6631453-chr7:6677284..6679167,4	K562	blood:
27	chr7:6656631..6659250-chr7:6667009..6671468,4	MCF-7	breast:
28	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
29	chr7:6666562..6671587-chr7:6674314..6680724,9	MCF-7	breast:
30	chr17:41465185..41465700-chr7:6676633..6677215,2	Hela-S3	cervix:
31	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
32	chr7:6677446..6679002-chr7:6745294..6747715,2	K562	blood:
33	chr7:6661077..6664696-chr7:6667812..6669863,3	MCF-7	breast:
34	chr7:6682112..6684474-chr7:6686272..6690280,3	MCF-7	breast:
35	chr7:6668305..6670110-chr7:6679585..6681865,2	MCF-7	breast:
36	chr17:57920745..57921576-chr7:6676970..6677850,2	HCT-116	colon:
37	chr7:6682551..6684434-chr7:6694308..6696080,2	MCF-7	breast:
38	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
39	chr7:6687023..6688997-chr7:6745010..6747605,2	K562	blood:
40	chr7:6570467..6572933-chr7:6675256..6676794,2	MCF-7	breast:
41	chr7:6652934..6655791-chr7:6675915..6678392,2	MCF-7	breast:
42	chr7:6683236..6686038-chr7:6768255..6771021,2	K562	blood:
43	chr7:6674209..6679608-chr7:6682918..6689628,9	K562	blood:
44	chr7:6615800..6617832-chr7:6677563..6680150,2	MCF-7	breast:
45	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
46	chr7:6680149..6683134-chr7:6689202..6690780,2	K562	blood:
47	chr7:6661901..6664151-chr7:6670252..6671986,3	MCF-7	breast:
48	chr7:6669640..6671625-chr7:6687041..6689974,2	MCF-7	breast:
49	chr7:6675962..6678642-chr7:6744432..6748032,4	MCF-7	breast:
50	chr7:6676193..6679067-chr7:6744810..6746794,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF853-2	chr7:6670130-6670199	ucscGeneNc_uc003sqr_1
2	lnc-ZNF853-2	chr7:6671200-6671264	ucscGeneNc_uc003sqr_1
3	lnc-ZNF853-2	chr7:6679361-6680635	ucscGeneNc_uc003sqr_1

No data

Variant related genes	Relation type
ZNF316	TF binding region
ENSG00000260054	TF binding region
ZNF316	CpG island
ENSG00000260054	CpG island
ENSG00000269781	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000260054	chromatin interactions
ENSG00000135482	chromatin interactions
ENSG00000232581	chromatin interactions
ENSG00000164631	chromatin interactions
ENSG00000187953	chromatin interactions
ENSG00000139641	chromatin interactions
ENSG00000236609	chromatin interactions
ENSG00000146576	chromatin interactions
ENSG00000205903	chromatin interactions
ENSG00000077150	chromatin interactions
ENSG00000215045	chromatin interactions
ENSG00000136247	chromatin interactions
ENSG00000136240	chromatin interactions

Extended variants
information (count: 1221 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2030798	chr7:6666501-6666502	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs375397886	chr7:6666505-6666506	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs558256999	chr7:6666532-6666533	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs374738051	chr7:6666539-6666540	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150217080	chr7:6666563-6666564	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs76062189	chr7:6666604-6666605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs538133470	chr7:6666620-6666621	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs138750210	chr7:6666650-6666651	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs61227395	chr7:6666654-6666655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs555383606	chr7:6666660-6666661	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117701984	chr7:6666706-6666707	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs145583775	chr7:6666737-6666738	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs192044631	chr7:6666760-6666761	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs560170200	chr7:6666786-6666787	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs572216416	chr7:6666803-6666804	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs373812953	chr7:6666820-6666821	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs545622449	chr7:6666852-6666853	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs148871432	chr7:6666897-6666898	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs528086426	chr7:6666940-6666941	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs183639098	chr7:6667078-6667079	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs370233708	chr7:6667079-6667080	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs76200811	chr7:6667100-6667101	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs550565680	chr7:6667111-6667112	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs562792625	chr7:6667145-6667146	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs188979600	chr7:6667157-6667158	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs548413818	chr7:6667167-6667168	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs546231934	chr7:6667170-6667171	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs533645011	chr7:6667249-6667250	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs572722891	chr7:6667267-6667268	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs552274673	chr7:6667280-6667281	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs111256424	chr7:6667286-6667287	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs537864446	chr7:6667303-6667304	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs556414434	chr7:6667309-6667310	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs574797525	chr7:6667335-6667336	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs184321455	chr7:6667359-6667360	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs138097564	chr7:6667377-6667378	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs557259691	chr7:6667390-6667391	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs188374629	chr7:6667469-6667470	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs142358271	chr7:6667556-6667557	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs564619449	chr7:6667557-6667558	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs369861350	chr7:6667561-6667562	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs576329556	chr7:6667600-6667601	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs543802478	chr7:6667669-6667670	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs144561655	chr7:6667678-6667679	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs561550188	chr7:6667679-6667680	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs530004397	chr7:6667695-6667696	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs548546884	chr7:6667701-6667702	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs191629260	chr7:6667719-6667720	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs73348716	chr7:6667734-6667735	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs538323301	chr7:6667735-6667736	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6656000-6666600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr7:6656000-6676000	Weak transcription	Psoas Muscle	Psoas
3	chr7:6656200-6669200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:6656200-6675800	Weak transcription	HSMM	muscle
5	chr7:6656600-6669200	Weak transcription	Fetal Heart	heart
6	chr7:6656800-6667000	Strong transcription	Fetal Stomach	stomach
7	chr7:6656800-6675800	Weak transcription	Fetal Brain Male	brain
8	chr7:6660200-6676000	Weak transcription	Colonic Mucosa	Colon
9	chr7:6661600-6669600	Weak transcription	HepG2	liver
10	chr7:6661800-6675800	Weak transcription	Pancreas	Pancrea
11	chr7:6661800-6676000	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr7:6661800-6676200	Weak transcription	Right Atrium	heart
13	chr7:6662200-6667800	Weak transcription	Esophagus	oesophagus
14	chr7:6662800-6676000	Weak transcription	Colon Smooth Muscle	Colon
15	chr7:6663200-6666800	Weak transcription	Skeletal Muscle Female	skeletal muscle
16	chr7:6663200-6667800	Weak transcription	Spleen	Spleen
17	chr7:6663200-6676000	Weak transcription	Brain Anterior Caudate	brain
18	chr7:6663200-6676000	Weak transcription	Rectal Smooth Muscle	rectum
19	chr7:6663400-6669800	Weak transcription	Fetal Intestine Small	intestine
20	chr7:6663600-6667400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr7:6663600-6669800	Weak transcription	Placenta Amnion	Placenta Amnion
22	chr7:6663800-6667400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr7:6663800-6667600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr7:6663800-6667800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr7:6663800-6668000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr7:6663800-6668200	Weak transcription	Adipose Nuclei	Adipose
27	chr7:6663800-6669600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr7:6663800-6669800	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr7:6663800-6676000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:6663800-6676000	Weak transcription	Brain Angular Gyrus	brain
31	chr7:6663800-6676000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr7:6663800-6676000	Weak transcription	Brain Substantia Nigra	brain
33	chr7:6663800-6676000	Weak transcription	Fetal Intestine Large	intestine
34	chr7:6663800-6676000	Weak transcription	Gastric	stomach
35	chr7:6663800-6676000	Weak transcription	Left Ventricle	heart
36	chr7:6663800-6676000	Weak transcription	Lung	lung
37	chr7:6663800-6676000	Weak transcription	Right Ventricle	heart
38	chr7:6663800-6676000	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr7:6664000-6668200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr7:6664000-6675800	Weak transcription	Duodenum Smooth Muscle	Duodenum
41	chr7:6664000-6676000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr7:6664200-6669800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:6664200-6676000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:6664200-6676000	Weak transcription	Ovary	ovary
45	chr7:6664400-6675200	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr7:6664400-6676000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr7:6665000-6668400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr7:6665200-6671200	Weak transcription	Aorta	Aorta
49	chr7:6665200-6675800	Weak transcription	Stomach Smooth Muscle	stomach
50	chr7:6665200-6676000	Weak transcription	Brain Germinal Matrix	brain

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