Variant report

Variant	esv2752139
Chromosome Location	chr7:10798492-10954219
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:841)
CpG islands
(count:306)
Chromatin interactive
region (count:74)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:841 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:10827093-10828575	K562	blood:	n/a	n/a
2	ARID3A	chr7:10824576-10825525	K562	blood:	n/a	n/a
3	ARID3A	chr7:10828806-10829422	K562	blood:	n/a	n/a
4	ARID3A	chr7:10819982-10820312	K562	blood:	n/a	n/a
5	ARID3A	chr7:10843350-10843838	K562	blood:	n/a	n/a
6	ARID3A	chr7:10807510-10807645	HepG2	liver:	n/a	n/a
7	ARID3A	chr7:10825950-10826234	K562	blood:	n/a	n/a
8	ARID3A	chr7:10820673-10821069	K562	blood:	n/a	n/a
9	ARID3A	chr7:10822610-10823962	K562	blood:	n/a	n/a
10	ARID3A	chr7:10819577-10819739	K562	blood:	n/a	n/a
11	ARID3A	chr7:10929010-10929223	HepG2	liver:	n/a	n/a
12	ATF1	chr7:10863783-10863987	K562	blood:	n/a	n/a
13	ATF1	chr7:10888418-10888488	K562	blood:	n/a	n/a
14	ATF2	chr7:10948088-10948631	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr7:10948090-10948701	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr7:10928900-10929340	GM12878	blood:	n/a	n/a
17	ATF3	chr7:10819432-10819699	K562	blood:	n/a	n/a
18	ATF3	chr7:10948157-10948481	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr7:10873756-10873763	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr7:10900192-10900543	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr7:10820003-10820227	K562	blood:	n/a	n/a
22	BACH1	chr7:10828799-10829186	K562	blood:	n/a	n/a
23	BACH1	chr7:10890798-10890815	K562	blood:	n/a	n/a
24	BATF	chr7:10877940-10878140	GM12878	blood:	n/a	chr7:10878032-10878042 chr7:10878031-10878042
25	BHLHE40	chr7:10843360-10843677	K562	blood:	n/a	n/a
26	BHLHE40	chr7:10819221-10820325	K562	blood:	n/a	n/a
27	BHLHE40	chr7:10829391-10829517	K562	blood:	n/a	n/a
28	BHLHE40	chr7:10929005-10929271	GM12878	blood:	n/a	n/a
29	CBX3	chr7:10819802-10820330	K562	blood:	n/a	n/a
30	CBX3	chr7:10843321-10843698	K562	blood:	n/a	n/a
31	CBX3	chr7:10798725-10799248	K562	blood:	n/a	n/a
32	CBX3	chr7:10798683-10799247	K562	blood:	n/a	n/a
33	CBX3	chr7:10951230-10951678	K562	blood:	n/a	n/a
34	CBX3	chr7:10819121-10820416	K562	blood:	n/a	n/a
35	CBX3	chr7:10798754-10799163	HCT-116	colon:	n/a	n/a
36	CBX3	chr7:10819371-10819744	K562	blood:	n/a	n/a
37	CCNT2	chr7:10819476-10819678	K562	blood:	n/a	n/a
38	CCNT2	chr7:10843396-10843653	K562	blood:	n/a	chr7:10843513-10843533
39	CEBPB	chr7:10829437-10829723	K562	blood:	n/a	chr7:10829690-10829703
40	CEBPB	chr7:10828661-10829138	K562	blood:	n/a	n/a
41	CEBPB	chr7:10894908-10895095	K562	blood:	n/a	chr7:10894983-10894994
42	CEBPB	chr7:10861689-10861980	K562	blood:	n/a	chr7:10861844-10861855 chr7:10861844-10861857
43	CEBPB	chr7:10880078-10880415	K562	blood:	n/a	n/a
44	CEBPB	chr7:10843332-10843713	K562	blood:	n/a	n/a
45	CEBPB	chr7:10945946-10946181	HepG2	liver:	n/a	n/a
46	CEBPB	chr7:10880116-10880399	IMR90	lung:	n/a	n/a
47	CEBPB	chr7:10861692-10861982	IMR90	lung:	n/a	chr7:10861844-10861855 chr7:10861844-10861857
48	CEBPB	chr7:10950556-10950747	HepG2	liver:	n/a	n/a
49	CEBPB	chr7:10839135-10839466	HepG2	liver:	n/a	chr7:10839197-10839208 chr7:10839283-10839294 chr7:10839282-10839295 chr7:10839282-10839293
50	CEBPB	chr7:10818880-10819256	K562	blood:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:10819513-10819563	PFSK-1	brain:	n/a
2	chr7:10819513-10819563	PFSK-1	brain:	n/a
3	chr7:10819051-10819101	HEK293	kidney:	embryo
4	chr7:10819513-10819563	HNPCEpiC	eye:	n/a
5	chr7:10819370-10819420	AG04449	skin:	fetal
6	chr7:10819632-10819682	NB4	blood:	n/a
7	chr7:10819370-10819420	MCF10A-Er-Src	breast:	n/a
8	chr7:10819051-10819101	RPTEC	kidney:	n/a
9	chr7:10819632-10819682	U87	brain:	n/a
10	chr7:10819513-10819563	HCT-116	colon:	n/a
11	chr7:10819513-10819563	Caco-2	colon:	n/a
12	chr7:10819370-10819420	IMR90	lung:	fetal
13	chr7:10819051-10819101	MCF-7	breast:	n/a
14	chr7:10819370-10819420	ovcar-3	ovarian:	n/a
15	chr7:10819051-10819101	HL-60	blood:	n/a
16	chr7:10819513-10819563	NH-A	brain:	n/a
17	chr7:10819513-10819563	T-47D	breast:	n/a
18	chr7:10819836-10819886	HL-60	blood:	n/a
19	chr7:10819370-10819420	HL-60	blood:	n/a
20	chr7:10819370-10819420	K562	blood:	n/a
21	chr7:10819836-10819886	Hepatocyte	liver:	n/a
22	chr7:10819513-10819563	AG09309	skin:	n/a
23	chr7:10819370-10819420	HRCEpiC	kidney:	n/a
24	chr7:10819632-10819682	IMR90	lung:	fetal
25	chr7:10819632-10819682	HNPCEpiC	eye:	n/a
26	chr7:10819051-10819101	BJ	skin:	n/a
27	chr7:10819632-10819682	AG04450	lung:	fetal
28	chr7:10819836-10819886	SK-N-SH_RA	brain:	n/a
29	chr7:10819632-10819682	BE2_C	brain:	n/a
30	chr7:10819370-10819420	AG09309	skin:	n/a
31	chr7:10819370-10819420	SKMC	muscle:	n/a
32	chr7:10819632-10819682	GM19239	blood:	n/a
33	chr7:10819370-10819420	HCM	heart:	n/a
34	chr7:10819836-10819886	A549	lung:	n/a
35	chr7:10819051-10819101	HCT-116	colon:	n/a
36	chr7:10819632-10819682	GM12878	blood:	n/a
37	chr7:10819836-10819886	BJ	skin:	n/a
38	chr7:10819632-10819682	GM06990	blood:	n/a
39	chr7:10819632-10819682	AoSMC	blood vessel:	n/a
40	chr7:10819632-10819682	K562	blood:	n/a
41	chr7:10819836-10819886	HAEpiC	amniotic membrane:	n/a
42	chr7:10819370-10819420	U87	brain:	n/a
43	chr7:10819836-10819886	NB4	blood:	n/a
44	chr7:10819836-10819886	HNPCEpiC	eye:	n/a
45	chr7:10819513-10819563	AG09319	gingival:	n/a
46	chr7:10819632-10819682	HRCEpiC	kidney:	n/a
47	chr7:10819051-10819101	AG09319	gingival:	n/a
48	chr7:10819051-10819101	PFSK-1	brain:	n/a
49	chr7:10819051-10819101	CMK	blood:	n/a
50	chr7:10819836-10819886	SAEC	small airway:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr7:10831578..10833139-chr7:10835403..10837636,2	K562	blood:
2	chr7:10827906..10830733-chr7:10877571..10879129,2	K562	blood:
3	chr15:44829060..44829617-chr7:10881734..10882714,2	Hela-S3	cervix:
4	chr7:10818173..10820348-chr7:10835092..10837253,2	K562	blood:
5	chr7:10837164..10840989-chr7:10841354..10845729,6	K562	blood:
6	chr7:10810774..10813337-chr7:10818545..10820723,2	K562	blood:
7	chr7:10903152..10905363-chr7:10907278..10909562,2	K562	blood:
8	chr7:10824928..10828971-chr7:10836340..10841175,4	K562	blood:
9	chr7:10910112..10911906-chr7:10912737..10915573,2	K562	blood:
10	chr7:10903863..10905750-chr7:10907380..10909562,2	K562	blood:
11	chr7:10768715..10771271-chr7:10816725..10820425,4	K562	blood:
12	chr7:10676395..10677225-chr7:10928650..10929592,2	K562	blood:
13	chr7:10810774..10813337-chr7:10818545..10820723,2	K562	blood:
14	chr7:10909984..10911612-chr7:10912737..10914507,2	K562	blood:
15	chr7:10795591..10798221-chr7:10854575..10857146,3	K562	blood:
16	chr7:10838575..10840856-chr7:10841977..10843988,2	MCF-7	breast:
17	chr7:10803747..10805701-chr7:10813863..10816423,2	K562	blood:
18	chr7:10831578..10833139-chr7:10835403..10837636,2	K562	blood:
19	chr7:10903152..10905363-chr7:10907278..10909562,2	K562	blood:
20	chr7:10838575..10840856-chr7:10841977..10843988,2	MCF-7	breast:
21	chr7:10908452..10910556-chr7:11019934..11022818,2	K562	blood:
22	chr7:10890558..10893396-chr7:10897220..10900177,2	K562	blood:
23	chr7:10903863..10905750-chr7:10907380..10909562,2	K562	blood:
24	chr7:10803159..10807219-chr7:10807656..10811292,5	K562	blood:
25	chr7:10947517..10950005-chr7:10956259..10958787,2	K562	blood:
26	chr5:16464666..16467634-chr7:10878203..10880591,2	MCF-7	breast:
27	chr7:10827906..10830733-chr7:10877571..10879129,2	K562	blood:
28	chr7:10816838..10819406-chr7:11013285..11015012,2	K562	blood:
29	chr3:73159945..73160606-chr7:10881714..10882734,5	HCT-116	colon:
30	chr7:10837164..10840989-chr7:10841354..10845729,6	K562	blood:
31	chr17:41463316..41465702-chr7:10880714..10882234,3	K562	blood:
32	chr7:10818173..10820348-chr7:10835092..10837253,2	K562	blood:
33	chr7:10807031..10808703-chr7:10828329..10831048,2	K562	blood:
34	chr7:10795829..10798121-chr7:10807049..10811087,3	K562	blood:
35	chr7:10824928..10828971-chr7:10836340..10841175,4	K562	blood:
36	chr7:10852219..10854827-chr7:10860395..10863241,2	K562	blood:
37	chr7:10890558..10893396-chr7:10897220..10900177,2	K562	blood:
38	chr7:10910112..10911906-chr7:10912737..10915573,2	K562	blood:
39	chr10:103124241..103125130-chr7:10881734..10882714,2	Hela-S3	cervix:
40	chr15:101368678..101369358-chr7:10860703..10861283,2	MCF-7	breast:
41	chr2:192281175..192282695-chr7:10880714..10882234,2	K562	blood:
42	chr7:10772404..10775050-chr7:10821026..10823931,2	K562	blood:
43	chr7:10909984..10911612-chr7:10912737..10914507,2	K562	blood:
44	chr7:10827479..10830753-chr7:10830945..10833884,5	K562	blood:
45	chr7:10852219..10854827-chr7:10860395..10863241,2	K562	blood:
46	chr7:10809012..10810687-chr7:10812271..10814019,2	K562	blood:
47	chr7:10778744..10781099-chr7:10818958..10821486,2	K562	blood:
48	chr7:10829022..10831509-chr7:11013327..11015576,2	K562	blood:
49	chr7:10818699..10822020-chr7:10830372..10832359,3	K562	blood:
50	chr7:10852190..10855109-chr7:10857378..10860919,3	K562	blood:

No data

Variant related genes	Relation type
ENSG00000201774	TF binding region
ENSG00000201774	CpG island
ENSG00000173545	chromatin interactions
ENSG00000189043	chromatin interactions
ENSG00000106443	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000179523	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000271185	chromatin interactions
ENSG00000222414	chromatin interactions
ENSG00000104131	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 3375 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:3375 , 50 per page) page: 1 2 3 4 5 6 7 ... 68

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10486095	chr7:10798492-10798493	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs533323087	chr7:10798500-10798501	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs185315107	chr7:10798538-10798539	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs551287562	chr7:10798543-10798544	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs567901754	chr7:10798567-10798568	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs17163527	chr7:10798619-10798620	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs553496639	chr7:10798669-10798670	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs143795919	chr7:10798673-10798674	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs534389496	chr7:10798721-10798722	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs372059611	chr7:10798730-10798731	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs557475828	chr7:10798764-10798765	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs577206646	chr7:10798768-10798769	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs147220409	chr7:10798773-10798774	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs556688194	chr7:10798781-10798782	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs140660808	chr7:10798813-10798814	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs551854917	chr7:10798832-10798833	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs12531565	chr7:10798843-10798844	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs532429514	chr7:10798850-10798851	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs559485438	chr7:10798914-10798915	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs34627222	chr7:10798936-10798937	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs528323616	chr7:10798978-10798979	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs545515531	chr7:10799006-10799007	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs557213841	chr7:10799015-10799016	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs192158607	chr7:10799027-10799028	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs531029903	chr7:10799030-10799031	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs183814202	chr7:10799037-10799038	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs569852255	chr7:10799062-10799063	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs567643415	chr7:10799092-10799093	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs75579513	chr7:10799093-10799094	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs144497955	chr7:10799133-10799134	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs566718785	chr7:10799186-10799187	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs144561939	chr7:10799206-10799207	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs370111407	chr7:10799249-10799250	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs187593296	chr7:10799262-10799263	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs572019322	chr7:10799271-10799272	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs148447514	chr7:10799283-10799284	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs536773979	chr7:10799298-10799299	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs73680912	chr7:10799341-10799342	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs191574814	chr7:10799371-10799372	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs536526450	chr7:10799402-10799403	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs553040131	chr7:10799409-10799410	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs183029662	chr7:10799417-10799418	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs142570604	chr7:10799425-10799426	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs554539803	chr7:10799431-10799432	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs116489416	chr7:10799438-10799439	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs575774689	chr7:10799452-10799453	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs186861929	chr7:10799459-10799460	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs557934804	chr7:10799489-10799490	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs150946540	chr7:10799539-10799540	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs17163529	chr7:10799568-10799569	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	22286061	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Medulloblastoma	17653508	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	18194544	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:10798200-10800200	ZNF genes & repeats	K562	blood
2	chr7:10800200-10803400	Weak transcription	K562	blood
3	chr7:10803400-10809000	Strong transcription	K562	blood
4	chr7:10807600-10808000	Enhancers	NH-A	brain
5	chr7:10809000-10814000	Weak transcription	K562	blood
6	chr7:10809200-10810600	Enhancers	Brain Substantia Nigra	brain
7	chr7:10809200-10810800	Enhancers	Brain Hippocampus Middle	brain
8	chr7:10809600-10810800	Enhancers	Brain Cingulate Gyrus	brain
9	chr7:10809800-10811000	Enhancers	Brain Angular Gyrus	brain
10	chr7:10810000-10811000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:10810000-10811000	Enhancers	Brain Inferior Temporal Lobe	brain
12	chr7:10812400-10813000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:10814000-10814200	Strong transcription	K562	blood
14	chr7:10814200-10814400	Genic enhancers	K562	blood
15	chr7:10814400-10814600	Strong transcription	K562	blood
16	chr7:10814600-10815800	Weak transcription	K562	blood
17	chr7:10815800-10817200	Active TSS	K562	blood
18	chr7:10817200-10818200	Weak transcription	K562	blood
19	chr7:10818200-10819200	Active TSS	K562	blood
20	chr7:10819200-10819600	Flanking Active TSS	K562	blood
21	chr7:10819400-10820200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:10819600-10820000	Active TSS	Spleen	Spleen
23	chr7:10819600-10821000	Active TSS	K562	blood
24	chr7:10820000-10820200	Flanking Active TSS	Spleen	Spleen
25	chr7:10821000-10821400	Enhancers	K562	blood
26	chr7:10821400-10822200	Weak transcription	K562	blood
27	chr7:10822200-10822800	Active TSS	K562	blood
28	chr7:10822800-10823800	Weak transcription	K562	blood
29	chr7:10823800-10826600	Active TSS	K562	blood
30	chr7:10826600-10827600	Flanking Active TSS	K562	blood
31	chr7:10827600-10828200	Active TSS	K562	blood
32	chr7:10828200-10829400	Flanking Active TSS	K562	blood
33	chr7:10828600-10829800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:10828800-10829400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr7:10829200-10829800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr7:10829400-10829600	Enhancers	K562	blood
37	chr7:10829400-10829800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr7:10829400-10829800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr7:10829800-10834000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr7:10834000-10834400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr7:10834000-10834400	Enhancers	NH-A	brain
42	chr7:10834000-10834600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:10834200-10834600	Enhancers	Muscle Satellite Cultured Cells	--
44	chr7:10836800-10837400	Enhancers	K562	blood
45	chr7:10837400-10837800	Active TSS	K562	blood
46	chr7:10837800-10838000	Enhancers	HSMM	muscle
47	chr7:10837800-10838200	Flanking Active TSS	K562	blood
48	chr7:10838200-10842400	Weak transcription	K562	blood
49	chr7:10840800-10841600	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr7:10841400-10843000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links