Variant report

Variant	nsv1029023
Chromosome Location	chr7:119292763-119606632
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1341)
CpG islands
(count:122)
Chromatin interactive
region (count:229)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1341 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:119485246-119485330	K562	blood:	n/a	n/a
2	ARID3A	chr7:119588383-119588467	K562	blood:	n/a	n/a
3	ARID3A	chr7:119603730-119604003	K562	blood:	n/a	n/a
4	ARID3A	chr7:119533898-119533920	K562	blood:	n/a	n/a
5	ARID3A	chr7:119565663-119566331	K562	blood:	n/a	n/a
6	ARID3A	chr7:119544471-119544634	K562	blood:	n/a	n/a
7	ARID3A	chr7:119545914-119546769	K562	blood:	n/a	n/a
8	ARID3A	chr7:119604894-119605665	K562	blood:	n/a	n/a
9	ARID3A	chr7:119547213-119547605	K562	blood:	n/a	n/a
10	ARID3A	chr7:119574813-119574830	K562	blood:	n/a	n/a
11	ARID3A	chr7:119585975-119586344	K562	blood:	n/a	n/a
12	ARID3A	chr7:119575623-119575727	HepG2	liver:	n/a	n/a
13	ARID3A	chr7:119533532-119533639	K562	blood:	n/a	n/a
14	ARID3A	chr7:119535268-119535593	K562	blood:	n/a	n/a
15	ARID3A	chr7:119583732-119584605	K562	blood:	n/a	n/a
16	ARID3A	chr7:119356600-119356718	K562	blood:	n/a	n/a
17	ARID3A	chr7:119575491-119576056	K562	blood:	n/a	n/a
18	ARID3A	chr7:119571360-119572258	K562	blood:	n/a	n/a
19	ARID3A	chr7:119556591-119556623	K562	blood:	n/a	n/a
20	ARID3A	chr7:119549177-119549427	K562	blood:	n/a	n/a
21	ATF1	chr7:119565968-119566309	K562	blood:	n/a	n/a
22	ATF1	chr7:119549049-119549443	K562	blood:	n/a	n/a
23	ATF1	chr7:119360724-119360869	K562	blood:	n/a	n/a
24	ATF1	chr7:119547275-119547621	K562	blood:	n/a	n/a
25	ATF1	chr7:119604972-119605649	K562	blood:	n/a	n/a
26	ATF1	chr7:119329630-119329700	K562	blood:	n/a	n/a
27	ATF1	chr7:119535148-119535329	K562	blood:	n/a	n/a
28	ATF1	chr7:119590901-119591026	K562	blood:	n/a	n/a
29	ATF2	chr7:119351098-119351553	GM12878	blood:	n/a	n/a
30	ATF2	chr7:119351112-119351541	GM12878	blood:	n/a	n/a
31	ATF3	chr7:119547664-119547998	K562	blood:	n/a	n/a
32	ATF3	chr7:119604903-119605339	K562	blood:	n/a	n/a
33	BACH1	chr7:119589003-119589869	K562	blood:	n/a	n/a
34	BACH1	chr7:119448882-119448897	K562	blood:	n/a	n/a
35	BACH1	chr7:119456600-119456624	K562	blood:	n/a	n/a
36	BATF	chr7:119351170-119351425	GM12878	blood:	n/a	chr7:119351322-119351330
37	BATF	chr7:119351259-119351432	GM12878	blood:	n/a	chr7:119351322-119351330
38	BATF	chr7:119321466-119321694	GM12878	blood:	n/a	n/a
39	BCL11A	chr7:119351161-119351439	GM12878	blood:	n/a	chr7:119351318-119351327
40	BCL11A	chr7:119297324-119297552	GM12878	blood:	n/a	n/a
41	BCLAF1	chr7:119351118-119351465	GM12878	blood:	n/a	chr7:119351318-119351327
42	BCLAF1	chr7:119588928-119590441	K562	blood:	n/a	n/a
43	BHLHE40	chr7:119578413-119578420	K562	blood:	n/a	n/a
44	BHLHE40	chr7:119566020-119566327	K562	blood:	n/a	n/a
45	BHLHE40	chr7:119549136-119549393	K562	blood:	n/a	n/a
46	CBX3	chr7:119509760-119510161	K562	blood:	n/a	n/a
47	CBX3	chr7:119524841-119525448	K562	blood:	n/a	n/a
48	CBX3	chr7:119565965-119566333	K562	blood:	n/a	n/a
49	CBX3	chr7:119590477-119591189	K562	blood:	n/a	n/a
50	CBX3	chr7:119565918-119566414	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:119590451-119590501	AoSMC	blood vessel:	n/a
2	chr7:119604878-119604928	NHBE	bronchial:	n/a
3	chr7:119604878-119604928	AG10803	skin:	n/a
4	chr7:119604878-119604928	HNPCEpiC	eye:	n/a
5	chr7:119590451-119590501	HEEpiC	esophagus:	n/a
6	chr7:119604878-119604928	NHDF-neo	bronchial:	n/a
7	chr7:119590451-119590501	SKMC	muscle:	n/a
8	chr7:119590451-119590501	ProgFib	skin:	n/a
9	chr7:119604878-119604928	HRE	kidney:	n/a
10	chr7:119590451-119590501	Jurkat	blood:	n/a
11	chr7:119590451-119590501	AG09309	skin:	n/a
12	chr7:119604878-119604928	U87	brain:	n/a
13	chr7:119590451-119590501	AG09319	gingival:	n/a
14	chr7:119590451-119590501	PrEC	prostate:	n/a
15	chr7:119604878-119604928	LNCaP	prostate:	n/a
16	chr7:119604878-119604928	HUVEC	blood vessel:	n/a
17	chr7:119590451-119590501	SK-N-SH_RA	brain:	n/a
18	chr7:119604878-119604928	PrEC	prostate:	n/a
19	chr7:119604878-119604928	HCF	heart:	n/a
20	chr7:119590451-119590501	GM19239	blood:	n/a
21	chr7:119604878-119604928	AG04450	lung:	fetal
22	chr7:119590451-119590501	AG04450	lung:	fetal
23	chr7:119590451-119590501	CMK	blood:	n/a
24	chr7:119590451-119590501	HCF	heart:	n/a
25	chr7:119604878-119604928	NB4	blood:	n/a
26	chr7:119604878-119604928	ECC-1	luminal epithelium:	n/a
27	chr7:119604878-119604928	SK-N-SH_RA	brain:	n/a
28	chr7:119604878-119604928	GM12878	blood:	n/a
29	chr7:119604878-119604928	SAEC	small airway:	n/a
30	chr7:119604878-119604928	Hela-S3	cervix:	n/a
31	chr7:119590451-119590501	NH-A	brain:	n/a
32	chr7:119604878-119604928	PANC-1	pancreas:	n/a
33	chr7:119590451-119590501	HIPEpiC	eye:	n/a
34	chr7:119604878-119604928	A549	lung:	n/a
35	chr7:119590451-119590501	PFSK-1	brain:	n/a
36	chr7:119590451-119590501	NT2-D1	testis:	n/a
37	chr7:119604878-119604928	BE2_C	brain:	n/a
38	chr7:119590451-119590501	GM12891	blood:	n/a
39	chr7:119604878-119604928	SK-N-MC	brain:	n/a
40	chr7:119590451-119590501	AG04449	skin:	fetal
41	chr7:119604878-119604928	HRPEpiC	eye:	n/a
42	chr7:119590451-119590501	Caco-2	colon:	n/a
43	chr7:119604878-119604928	GM19239	blood:	n/a
44	chr7:119604878-119604928	HCPEpiC	choroid plexus:	n/a
45	chr7:119604878-119604928	K562	blood:	n/a
46	chr7:119604878-119604928	NT2-D1	testis:	n/a
47	chr7:119604878-119604928	AG09319	gingival:	n/a
48	chr7:119590451-119590501	AG10803	skin:	n/a
49	chr7:119604878-119604928	T-47D	breast:	n/a
50	chr7:119604878-119604928	RPTEC	kidney:	n/a

(count:229 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr7:119589512..119591360-chr7:119594151..119597360,3	K562	blood:
2	chr7:119383218..119386091-chr7:119386979..119388711,2	K562	blood:
3	chr7:119501656..119503413-chr7:119506676..119508249,2	K562	blood:
4	chr7:119531336..119533343-chr7:119587590..119589885,2	K562	blood:
5	chr7:119368480..119370359-chr7:119372677..119374451,2	K562	blood:
6	chr7:119596097..119601852-chr7:119602330..119605666,5	K562	blood:
7	chr7:119564930..119567525-chr7:119586667..119589307,3	K562	blood:
8	chr7:119533151..119535556-chr7:119574432..119576390,2	K562	blood:
9	chr7:119573958..119576750-chr7:119589483..119591512,2	K562	blood:
10	chr7:119548507..119550960-chr7:119636367..119638999,2	K562	blood:
11	chr7:119547567..119549067-chr7:119606535..119609324,2	K562	blood:
12	chr7:119511194..119513890-chr7:119518810..119520879,2	K562	blood:
13	chr7:119397490..119400025-chr7:119421872..119424720,2	MCF-7	breast:
14	chr7:119402295..119404288-chr7:119404943..119407340,2	K562	blood:
15	chr7:119510525..119513313-chr7:119545335..119546843,2	K562	blood:
16	chr7:119473939..119476344-chr7:119479412..119481119,2	K562	blood:
17	chr7:119570469..119574295-chr7:119575625..119578871,3	K562	blood:
18	chr7:119558453..119560333-chr7:119575522..119578295,2	K562	blood:
19	chr7:119551448..119555226-chr7:119556760..119560982,4	K562	blood:
20	chr7:119413236..119417031-chr7:119417738..119421768,6	K562	blood:
21	chr7:119570545..119573012-chr7:119573015..119575598,2	K562	blood:
22	chr7:119308246..119311748-chr7:119315573..119317458,3	K562	blood:
23	chr7:119487540..119490536-chr7:119492292..119494646,2	K562	blood:
24	chr7:119397490..119400025-chr7:119421872..119424720,2	MCF-7	breast:
25	chr7:119595929..119598016-chr7:119599722..119602227,2	K562	blood:
26	chr7:119420199..119422229-chr7:119425148..119427831,2	K562	blood:
27	chr7:119487540..119490536-chr7:119492292..119494646,2	K562	blood:
28	chr7:119572787..119576146-chr7:119578976..119581903,5	K562	blood:
29	chr7:119535257..119536915-chr7:119542608..119545152,2	K562	blood:
30	chr7:119603198..119605328-chr7:119613370..119615944,2	K562	blood:
31	chr7:119596097..119599917-chr7:119604166..119607181,3	K562	blood:
32	chr7:119464670..119466870-chr7:119472485..119474183,2	K562	blood:
33	chr1:121484535..121485269-chr7:119474518..119475464,2	MCF-7	breast:
34	chr7:119573362..119575942-chr7:119596349..119600152,3	K562	blood:
35	chr7:119527652..119529791-chr7:119534255..119537137,2	K562	blood:
36	chr7:119516671..119518877-chr7:119519641..119522411,2	K562	blood:
37	chr7:119489803..119491919-chr7:119544731..119547433,2	K562	blood:
38	chr7:119561524..119564382-chr7:119564905..119567041,3	K562	blood:
39	chr7:119452460..119454329-chr7:119545907..119547422,2	K562	blood:
40	chr7:119544182..119546756-chr7:119562620..119564769,3	K562	blood:
41	chr7:119410529..119413456-chr7:119422041..119425141,3	K562	blood:
42	chr7:119573034..119574677-chr7:119575228..119577665,3	K562	blood:
43	chr7:119348460..119350527-chr7:119352829..119355249,2	K562	blood:
44	chr7:119528303..119529981-chr7:119532634..119534210,2	K562	blood:
45	chr7:119551448..119554657-chr7:119557824..119560982,4	K562	blood:
46	chr7:119510969..119512779-chr7:119515094..119517064,2	K562	blood:
47	chr7:119558453..119560333-chr7:119575522..119578295,2	K562	blood:
48	chr7:119544182..119546756-chr7:119562620..119564769,3	K562	blood:
49	chr7:119364396..119367239-chr7:119368438..119370916,2	K562	blood:
50	chr7:119346390..119349043-chr7:119407382..119409874,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN12-4	chr7:119547347-119547429	XLOC_006580
2	lnc-TSPAN12-8	chr7:119322820-119322866	NONHSAT122984
3	lnc-KCND2-2	chr7:119348262-119348369	NONHSAT122985
4	lnc-KCND2-2	chr7:119344514-119347011	NONHSAT122985
5	lnc-TSPAN12-4	chr7:119390869-119392229	XLOC_006580
6	lnc-TSPAN12-4	chr7:119440870-119440928	XLOC_006580
7	lnc-TSPAN12-4	chr7:119344610-119345026	XLOC_006580
8	lnc-TSPAN12-4	chr7:119440870-119440928	XLOC_006580
9	lnc-TSPAN12-4	chr7:119422338-119422411	XLOC_006580
10	lnc-TSPAN12-4	chr7:119547347-119547429	XLOC_006580
11	lnc-TSPAN12-8	chr7:119321046-119322265	NONHSAT122984

No data

Variant related genes	Relation type
ENSG00000225546	TF binding region
ENSG00000225546	CpG island
ENSG00000225546	chromatin interactions
ENSG00000105254	chromatin interactions
ENSG00000105258	chromatin interactions
PDE12	miRNA target sites
HOXC8	miRNA target sites

Extended variants
information (count: 9507 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:9507 , 50 per page) page: 1 2 3 4 5 6 7 ... 191

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147515196	chr7:119292802-119292803	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs565353533	chr7:119292857-119292858	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs185212807	chr7:119292858-119292859	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs28600065	chr7:119292859-119292860	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs190502880	chr7:119292870-119292871	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs538026814	chr7:119292889-119292890	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs551415158	chr7:119293010-119293011	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs549411997	chr7:119293069-119293070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs28549838	chr7:119293105-119293106	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs530440135	chr7:119293147-119293148	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs534007957	chr7:119293163-119293164	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs139397003	chr7:119293183-119293184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs577121752	chr7:119293190-119293191	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs150069593	chr7:119293219-119293220	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs182212231	chr7:119293230-119293231	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs576370028	chr7:119293233-119293234	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs144885657	chr7:119293258-119293259	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs375439338	chr7:119293299-119293300	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs561975782	chr7:119293311-119293312	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs149098250	chr7:119299656-119299657	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567281910	chr7:119299675-119299676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs561095856	chr7:119299732-119299733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs574788324	chr7:119299752-119299753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540528858	chr7:119299762-119299763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs373983460	chr7:119299763-119299764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs560840850	chr7:119299782-119299783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs532563169	chr7:119299839-119299840	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs191140836	chr7:119299845-119299846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564622665	chr7:119299876-119299877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73485193	chr7:119299880-119299881	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs143133523	chr7:119299891-119299892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113696204	chr7:119299898-119299899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs74302538	chr7:119299907-119299908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs529704367	chr7:119299941-119299942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs188439368	chr7:119299949-119299950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs552387130	chr7:119299958-119299959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs10085639	chr7:119299978-119299979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566821983	chr7:119299984-119299985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs538829373	chr7:119300013-119300014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140401660	chr7:119300049-119300050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71569009	chr7:119300068-119300069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs569354590	chr7:119300077-119300078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376236570	chr7:119300078-119300079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs72055685	chr7:119300092-119300093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538305677	chr7:119300095-119300096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs60854670	chr7:119300100-119300101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs555052182	chr7:119300122-119300123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs112643283	chr7:119300204-119300205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs540666707	chr7:119300247-119300248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs192902013	chr7:119300285-119300286	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	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
Lung cancer	18438408	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute myeloid leukemia	21251322	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
Biliary cancer	19435499	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Prostate cancer	23792589	CNVD
Adenocarcinoma	21044232	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Non-small cell lung cancer	19889201	CNVD
Acute myeloid leukemia	18000384	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Metastatic melanoma	18483359	CNVD
Autism	18414403	CNVD
Autism	19401682	CNVD
Autism	19546859	CNVD
Schizophrenia	19546859	CNVD
Tourette syndrome	19546859	CNVD
Melanoma	19188590	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	22286061	CNVD
Glioblastoma multiforme	21922591	CNVD
Hepatocellular carcinoma	16785998	CNVD
Glioblastoma multiforme	18628472	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18194544	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:119292800-119293400	ZNF genes & repeats	K562	blood
2	chr7:119299600-119300400	Enhancers	Fetal Heart	heart
3	chr7:119304000-119305400	Enhancers	HUVEC	blood vessel
4	chr7:119304200-119306200	Enhancers	Muscle Satellite Cultured Cells	--
5	chr7:119304200-119306400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr7:119304400-119304800	Enhancers	NH-A	brain
7	chr7:119304400-119305200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr7:119304400-119305200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr7:119304400-119306200	Enhancers	HSMM	muscle
10	chr7:119304400-119306400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:119304600-119305200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr7:119304800-119305800	Weak transcription	NH-A	brain
13	chr7:119304800-119306000	Enhancers	Osteobl	bone
14	chr7:119305200-119306000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr7:119305200-119306000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:119305600-119306200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr7:119305800-119306400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
18	chr7:119306000-119306200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr7:119306000-119306200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr7:119306000-119306200	Enhancers	NH-A	brain
21	chr7:119311000-119326000	Weak transcription	K562	blood
22	chr7:119324200-119325600	Enhancers	Muscle Satellite Cultured Cells	--
23	chr7:119324200-119326200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr7:119325200-119325800	Enhancers	Osteobl	bone
25	chr7:119325400-119326200	Enhancers	Fetal Brain Female	brain
26	chr7:119326000-119326200	Enhancers	Fetal Lung	lung
27	chr7:119326000-119326600	Enhancers	K562	blood
28	chr7:119328400-119329600	Enhancers	Fetal Lung	lung
29	chr7:119341000-119341200	Weak transcription	K562	blood
30	chr7:119341400-119341800	ZNF genes & repeats	K562	blood
31	chr7:119345800-119346800	ZNF genes & repeats	K562	blood
32	chr7:119345800-119347000	Enhancers	Dnd41	blood
33	chr7:119346200-119347000	Enhancers	Fetal Heart	heart
34	chr7:119346400-119346800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr7:119346400-119346800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr7:119346800-119347200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr7:119346800-119348800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
38	chr7:119346800-119364200	Weak transcription	K562	blood
39	chr7:119347200-119347400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr7:119347400-119348600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr7:119348800-119349400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr7:119349000-119349200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
43	chr7:119351000-119351600	Active TSS	GM12878-XiMat	blood
44	chr7:119359000-119360600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr7:119359400-119362000	Enhancers	HUVEC	blood vessel
46	chr7:119360200-119360600	Enhancers	NHDF-Ad	bronchial
47	chr7:119360200-119361400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr7:119360200-119362400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr7:119360400-119361400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr7:119360400-119361600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links