Variant report

Variant	nsv889385
Chromosome Location	chr7:145617629-145803095
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:940)
CpG islands
(count:244)
Chromatin interactive
region (count:79)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:940 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:145703778-145703907	K562	blood:	n/a	n/a
2	ARID3A	chr7:145750569-145750925	K562	blood:	n/a	n/a
3	ARID3A	chr7:145755180-145755400	K562	blood:	n/a	n/a
4	ARID3A	chr7:145677810-145677911	K562	blood:	n/a	n/a
5	ARID3A	chr7:145772258-145772458	K562	blood:	n/a	n/a
6	ARID3A	chr7:145652488-145652580	K562	blood:	n/a	n/a
7	ARID3A	chr7:145787264-145787483	HepG2	liver:	n/a	n/a
8	ARID3A	chr7:145787152-145787489	K562	blood:	n/a	n/a
9	ATF1	chr7:145699648-145699984	K562	blood:	n/a	n/a
10	ATF1	chr7:145717949-145718148	K562	blood:	n/a	n/a
11	ATF1	chr7:145728285-145728287	K562	blood:	n/a	n/a
12	ATF1	chr7:145750609-145750997	K562	blood:	n/a	n/a
13	ATF1	chr7:145775000-145775187	K562	blood:	n/a	n/a
14	ATF3	chr7:145750662-145750929	K562	blood:	n/a	n/a
15	ATF3	chr7:145716456-145716610	K562	blood:	n/a	n/a
16	ATF3	chr7:145683356-145683677	K562	blood:	n/a	n/a
17	BACH1	chr7:145642174-145642233	K562	blood:	n/a	n/a
18	BACH1	chr7:145750738-145750913	K562	blood:	n/a	n/a
19	BACH1	chr7:145686566-145686880	K562	blood:	n/a	n/a
20	BACH1	chr7:145727177-145727179	K562	blood:	n/a	n/a
21	BATF	chr7:145694359-145694555	GM12878	blood:	n/a	n/a
22	BATF	chr7:145694357-145694559	GM12878	blood:	n/a	n/a
23	BCL11A	chr7:145694347-145694680	GM12878	blood:	n/a	n/a
24	BCL11A	chr7:145694365-145694584	GM12878	blood:	n/a	n/a
25	BHLHE40	chr7:145683463-145683590	K562	blood:	n/a	n/a
26	BHLHE40	chr7:145755118-145755377	K562	blood:	n/a	n/a
27	BHLHE40	chr7:145750584-145750950	K562	blood:	n/a	n/a
28	BHLHE40	chr7:145699653-145700059	K562	blood:	n/a	n/a
29	BHLHE40	chr7:145694345-145694571	HepG2	liver:	n/a	n/a
30	BHLHE40	chr7:145660449-145660549	K562	blood:	n/a	n/a
31	BHLHE40	chr7:145719613-145719737	K562	blood:	n/a	n/a
32	BHLHE40	chr7:145793673-145793674	K562	blood:	n/a	n/a
33	BHLHE40	chr7:145699695-145700051	GM12878	blood:	n/a	n/a
34	BHLHE40	chr7:145621411-145621433	K562	blood:	n/a	n/a
35	BRCA1	chr7:145787246-145787465	H1-hESC	embryonic stem cell:	n/a	chr7:145787445-145787452
36	CBX3	chr7:145716048-145716747	K562	blood:	n/a	n/a
37	CBX3	chr7:145750559-145750949	K562	blood:	n/a	n/a
38	CCNT2	chr7:145682971-145683682	K562	blood:	n/a	n/a
39	CCNT2	chr7:145750619-145750985	K562	blood:	n/a	n/a
40	CCNT2	chr7:145789588-145789669	K562	blood:	n/a	n/a
41	CCNT2	chr7:145681997-145682076	K562	blood:	n/a	n/a
42	CCNT2	chr7:145796377-145796527	K562	blood:	n/a	n/a
43	CEBPB	chr7:145621118-145621318	K562	blood:	n/a	n/a
44	CEBPB	chr7:145767411-145767739	HepG2	liver:	n/a	chr7:145767547-145767560 chr7:145767601-145767614 chr7:145767548-145767559
45	CEBPB	chr7:145728016-145728266	K562	blood:	n/a	chr7:145728149-145728162 chr7:145728149-145728162
46	CEBPB	chr7:145770729-145770944	A549	lung:	n/a	n/a
47	CEBPB	chr7:145654608-145654863	A549	lung:	n/a	chr7:145654743-145654754
48	CEBPB	chr7:145635143-145635267	HepG2	liver:	n/a	chr7:145635173-145635184
49	CEBPB	chr7:145694376-145694541	K562	blood:	n/a	n/a
50	CEBPB	chr7:145767377-145767714	IMR90	lung:	n/a	chr7:145767547-145767560 chr7:145767601-145767614 chr7:145767548-145767559

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:145689965-145690015	AG04450	lung:	fetal
2	chr7:145716504-145716554	SK-N-SH_RA	brain:	n/a
3	chr7:145740788-145740838	RPTEC	kidney:	n/a
4	chr7:145689965-145690015	LNCaP	prostate:	n/a
5	chr7:145716504-145716554	HRPEpiC	eye:	n/a
6	chr7:145740788-145740838	GM12878	blood:	n/a
7	chr7:145716504-145716554	RPTEC	kidney:	n/a
8	chr7:145716614-145716664	Hepatocyte	liver:	n/a
9	chr7:145716614-145716664	HRPEpiC	eye:	n/a
10	chr7:145716504-145716554	HEK293	kidney:	embryo
11	chr7:145716504-145716554	CMK	blood:	n/a
12	chr7:145689965-145690015	SK-N-SH	brain:	n/a
13	chr7:145716614-145716664	BE2_C	brain:	n/a
14	chr7:145689965-145690015	PrEC	prostate:	n/a
15	chr7:145689965-145690015	ovcar-3	ovarian:	n/a
16	chr7:145740788-145740838	GM12892	blood:	n/a
17	chr7:145716504-145716554	HCPEpiC	choroid plexus:	n/a
18	chr7:145716614-145716664	PANC-1	pancreas:	n/a
19	chr7:145716614-145716664	NB4	blood:	n/a
20	chr7:145716614-145716664	CMK	blood:	n/a
21	chr7:145716614-145716664	LNCaP	prostate:	n/a
22	chr7:145716614-145716664	HEEpiC	esophagus:	n/a
23	chr7:145716504-145716554	BJ	skin:	n/a
24	chr7:145689965-145690015	HepG2	liver:	n/a
25	chr7:145716614-145716664	K562	blood:	n/a
26	chr7:145689965-145690015	A549	lung:	n/a
27	chr7:145740788-145740838	HRE	kidney:	n/a
28	chr7:145716614-145716664	MCF-7	breast:	n/a
29	chr7:145740788-145740838	HAEpiC	amniotic membrane:	n/a
30	chr7:145740788-145740838	NHDF-neo	bronchial:	n/a
31	chr7:145716504-145716554	AG09309	skin:	n/a
32	chr7:145716614-145716664	GM06990	blood:	n/a
33	chr7:145716504-145716554	ECC-1	luminal epithelium:	n/a
34	chr7:145740788-145740838	HepG2	liver:	n/a
35	chr7:145716504-145716554	ProgFib	skin:	n/a
36	chr7:145716504-145716554	IMR90	lung:	fetal
37	chr7:145689965-145690015	AG10803	skin:	n/a
38	chr7:145716504-145716554	GM12891	blood:	n/a
39	chr7:145740788-145740838	H1-hESC	embryonic stem cell:	embryo
40	chr7:145716504-145716554	AG04450	lung:	fetal
41	chr7:145716504-145716554	HUVEC	blood vessel:	n/a
42	chr7:145689965-145690015	NHBE	bronchial:	n/a
43	chr7:145716504-145716554	AoSMC	blood vessel:	n/a
44	chr7:145689965-145690015	RPTEC	kidney:	n/a
45	chr7:145716614-145716664	HCM	heart:	n/a
46	chr7:145716504-145716554	PANC-1	pancreas:	n/a
47	chr7:145740788-145740838	GM19239	blood:	n/a
48	chr7:145716614-145716664	HAEpiC	amniotic membrane:	n/a
49	chr7:145716614-145716664	Caco-2	colon:	n/a
50	chr7:145716504-145716554	AG04449	skin:	fetal

(count:79 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:145794339..145796121-chr7:145802069..145803645,2	K562	blood:
2	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:
3	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
4	chr7:145757899..145760042-chr7:145772123..145774268,2	K562	blood:
5	chr7:145733955..145735465-chr7:145739918..145741433,2	K562	blood:
6	chr7:144551617..144552520-chr7:145786903..145787735,4	MCF-7	breast:
7	chr7:145749911..145752197-chr7:145756067..145758121,2	K562	blood:
8	chr7:145620799..145623095-chr7:145631387..145633696,2	K562	blood:
9	chr7:145614214..145615977-chr7:145619608..145621998,3	K562	blood:
10	chr7:145623731..145626417-chr7:145628652..145631149,2	K562	blood:
11	chr7:145728196..145729845-chr7:145732878..145734449,2	K562	blood:
12	chr7:145757899..145760042-chr7:145772123..145774268,2	K562	blood:
13	chr7:145680328..145682466-chr7:145758892..145760742,2	K562	blood:
14	chr7:145693446..145695856-chr7:145705246..145708235,3	K562	blood:
15	chr7:145638170..145640134-chr7:145641870..145644599,2	K562	blood:
16	chr7:145623731..145626417-chr7:145628652..145631149,2	K562	blood:
17	chr7:145651291..145652811-chr7:145655164..145657985,2	K562	blood:
18	chr7:145716150..145718866-chr7:145724746..145727382,4	K562	blood:
19	chr7:145650881..145653959-chr7:145655164..145657985,4	K562	blood:
20	chr7:145721579..145724410-chr7:145727561..145729692,3	K562	blood:
21	chr7:145679343..145681995-chr7:145683818..145685327,2	K562	blood:
22	chr7:145704641..145707485-chr7:145707900..145710506,2	K562	blood:
23	chr7:145782508..145785032-chr7:145801785..145804184,2	K562	blood:
24	chr7:145716150..145718866-chr7:145724746..145727382,4	K562	blood:
25	chr7:145709801..145711953-chr7:145718759..145720900,2	K562	blood:
26	chr7:145782097..145783756-chr7:145785466..145787437,2	K562	blood:
27	chr7:145620799..145622783-chr7:145631883..145633696,2	K562	blood:
28	chr7:145794339..145796121-chr7:145802069..145803645,2	K562	blood:
29	chr7:145620799..145622783-chr7:145631883..145633696,2	K562	blood:
30	chr7:145747031..145750592-chr7:145750800..145754125,3	K562	blood:
31	chr7:145696018..145698429-chr7:145703495..145706180,2	K562	blood:
32	chr7:145749911..145752197-chr7:145756067..145758121,2	K562	blood:
33	chr7:145716150..145718502-chr7:145724762..145727451,3	K562	blood:
34	chr7:145640094..145641820-chr7:145645010..145646727,2	K562	blood:
35	chr7:145697305..145699991-chr7:145700087..145702652,2	K562	blood:
36	chr7:145774442..145776114-chr7:145776448..145779399,2	K562	blood:
37	chr7:145765986..145768873-chr7:145770171..145772250,2	K562	blood:
38	chr7:145771822..145774419-chr7:145775630..145778255,2	K562	blood:
39	chr7:144733716..144734359-chr7:145787136..145787836,2	MCF-7	breast:
40	chr7:145709801..145711953-chr7:145718759..145720900,2	K562	blood:
41	chr7:145640094..145641820-chr7:145645010..145646727,2	K562	blood:
42	chr7:145691152..145693851-chr7:145700419..145703123,2	K562	blood:
43	chr7:145721579..145724410-chr7:145727561..145729692,3	K562	blood:
44	chr7:144712868..144713384-chr7:145787231..145787880,2	MCF-7	breast:
45	chr7:145697305..145699991-chr7:145700087..145702652,2	K562	blood:
46	chr7:145650881..145653959-chr7:145655164..145657985,4	K562	blood:
47	chr7:145782508..145785032-chr7:145801785..145804184,2	K562	blood:
48	chr7:144733417..144734684-chr7:145786550..145787817,10	MCF-7	breast:
49	chr7:145765986..145768873-chr7:145770171..145772250,2	K562	blood:
50	chr7:145706930..145710318-chr7:145716575..145718700,3	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNTNAP2-4	chr7:145747160-145747457	NONHSAT123944
2	lnc-CNTNAP2-3	chr7:145777121-145777289	NONHSAT123945
3	lnc-CNTNAP2-3	chr7:145747717-145747809	NONHSAT123945
4	lnc-CNTNAP2-2	chr7:145793180-145793471	NONHSAT123946

No data

Variant related genes	Relation type
RN7SL207P	TF binding region
RN7SL207P	CpG island
ENSG00000264018	chromatin interactions

Extended variants
information (count: 2727 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:2727 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7780753	chr7:145617629-145617630	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs565229472	chr7:145617701-145617702	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs530948224	chr7:145617718-145617719	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs538848016	chr7:145617723-145617724	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs370879305	chr7:145617736-145617737	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs73462838	chr7:145617757-145617758	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs536210887	chr7:145617780-145617781	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs554304227	chr7:145617849-145617850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs187875482	chr7:145617862-145617863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111325007	chr7:145617878-145617879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs553260316	chr7:145617900-145617901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs148698379	chr7:145617962-145617963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs545217951	chr7:145617983-145617984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs193093091	chr7:145617989-145617990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575366030	chr7:145618015-145618016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs564405133	chr7:145618026-145618027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542983679	chr7:145618096-145618097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528635595	chr7:145618138-145618139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs202047435	chr7:145618156-145618157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35930585	chr7:145618157-145618158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370931905	chr7:145618170-145618171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs386360238	chr7:145618171-145618172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78625637	chr7:145618172-145618173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529892985	chr7:145618187-145618188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs71175624	chr7:145618188-145618189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs540117212	chr7:145618215-145618216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548101787	chr7:145618222-145618223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141257589	chr7:145618247-145618248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs532319492	chr7:145618258-145618259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60473071	chr7:145618295-145618296	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs568959068	chr7:145618399-145618400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs71991750	chr7:145618400-145618401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs60692229	chr7:145618412-145618413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199898359	chr7:145618413-145618414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61281846	chr7:145618414-145618415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185848772	chr7:145618445-145618446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs139675619	chr7:145618540-145618541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs367569894	chr7:145618565-145618566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs67904872	chr7:145618569-145618570	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs188312030	chr7:145618630-145618631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192212153	chr7:145618634-145618635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554353350	chr7:145618640-145618641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184408770	chr7:145618654-145618655	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557158578	chr7:145618661-145618662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370678614	chr7:145618671-145618672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575688841	chr7:145618692-145618693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs542791845	chr7:145618731-145618732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555052272	chr7:145618755-145618756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs73738459	chr7:145618796-145618797	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs534755729	chr7:145618831-145618832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
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
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	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
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Glioblastoma multiforme	18628472	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	16272173	CNVD
Myxofibrosarcoma	16751306	CNVD
Stuttering	21108403	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17133270	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Pancreatitis	21956041	CNVD
Acute myeloid leukemia	16864856	CNVD
Gastric cancer	16891809	CNVD
Lung cancer	17086460	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Cancer	20164920	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20808228	CNVD
Schizophrenia	20838587	CNVD
Schizophrenia	20718829	CNVD
Neuropsychiatric disorder	21827697	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145617200-145617800	ZNF genes & repeats	K562	blood
2	chr7:145617800-145621000	Weak transcription	K562	blood
3	chr7:145619200-145619600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr7:145621000-145621400	ZNF genes & repeats	K562	blood
5	chr7:145621400-145623600	Weak transcription	K562	blood
6	chr7:145623600-145624200	ZNF genes & repeats	K562	blood
7	chr7:145624200-145632400	Weak transcription	K562	blood
8	chr7:145626200-145627000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:145629000-145629600	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr7:145629200-145630000	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr7:145629400-145630000	Enhancers	H1 Cell Line	embryonic stem cell
12	chr7:145629400-145630000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr7:145629400-145630000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr7:145629400-145630000	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr7:145629400-145630200	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr7:145629800-145630200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr7:145630000-145634800	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr7:145630000-145634800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr7:145630000-145635000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr7:145634600-145635000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr7:145634800-145635200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr7:145634800-145635200	ZNF genes & repeats	K562	blood
23	chr7:145634800-145635400	Enhancers	H1 Cell Line	embryonic stem cell
24	chr7:145634800-145635400	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr7:145635000-145635200	Enhancers	H9 Cell Line	embryonic stem cell
26	chr7:145635000-145635400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr7:145635000-145635400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:145635000-145635400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr7:145635000-145635600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr7:145635200-145635600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chr7:145640200-145640400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr7:145640600-145640800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr7:145648200-145648600	Enhancers	Fetal Lung	lung
34	chr7:145648600-145649600	Weak transcription	Fetal Lung	lung
35	chr7:145649600-145649800	Enhancers	Fetal Lung	lung
36	chr7:145654400-145655000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr7:145658000-145660800	Weak transcription	K562	blood
38	chr7:145676800-145682600	Weak transcription	K562	blood
39	chr7:145679000-145679600	Enhancers	Brain Cingulate Gyrus	brain
40	chr7:145682600-145683800	Enhancers	K562	blood
41	chr7:145683000-145683800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:145683600-145684000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr7:145683800-145686800	Weak transcription	K562	blood
44	chr7:145686800-145687000	ZNF genes & repeats	K562	blood
45	chr7:145687000-145694000	Weak transcription	K562	blood
46	chr7:145698800-145700600	Enhancers	Primary hematopoietic stem cells	blood
47	chr7:145699400-145700000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr7:145699400-145700000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr7:145699400-145700400	Enhancers	Primary B cells from peripheral blood	blood
50	chr7:145699400-145700400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links