Variant report

Variant	nsv527833
Chromosome Location	chr7:12632085-12644502
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:84)
CpG islands
(count:61)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:84 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr7:12640956-12641205	GM12878	blood:	n/a	n/a
2	BHLHE40	chr7:12634844-12635148	K562	blood:	n/a	n/a
3	CBX3	chr7:12642012-12642335	K562	blood:	n/a	n/a
4	CBX3	chr7:12633685-12634028	K562	blood:	n/a	n/a
5	CBX3	chr7:12641946-12642277	K562	blood:	n/a	n/a
6	CEBPB	chr7:12642095-12642155	K562	blood:	n/a	n/a
7	CHD2	chr7:12633841-12633874	K562	blood:	n/a	n/a
8	CTCF	chr7:12634806-12634856	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr7:12634820-12634970	HepG2	liver:	n/a	n/a
10	CTCF	chr7:12634700-12634850	Caco-2	colon:	n/a	n/a
11	CTCF	chr7:12636140-12636290	GM12873	blood:	n/a	n/a
12	EP300	chr7:12634853-12635135	K562	blood:	n/a	n/a
13	EP300	chr7:12634288-12634295	K562	blood:	n/a	n/a
14	EP300	chr7:12642195-12642217	K562	blood:	n/a	n/a
15	EP300	chr7:12634827-12635144	T-47D	breast:	n/a	n/a
16	ESR1	chr7:12634755-12635233	T-47D	breast:	n/a	n/a
17	ESR1	chr7:12634776-12635193	T-47D	breast:	n/a	n/a
18	ESR1	chr7:12634743-12635231	T-47D	breast:	n/a	n/a
19	ESR1	chr7:12634865-12635094	T-47D	breast:	n/a	n/a
20	ESR1	chr7:12634678-12635215	T-47D	breast:	n/a	n/a
21	ESR1	chr7:12634718-12635207	T-47D	breast:	n/a	n/a
22	FOS	chr7:12636217-12636404	MCF10A-Er-Src	breast:	n/a	chr7:12636253-12636261 chr7:12636252-12636262
23	FOS	chr7:12636112-12636412	MCF10A-Er-Src	breast:	n/a	chr7:12636253-12636261 chr7:12636252-12636262
24	FOS	chr7:12633839-12634059	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr7:12636151-12636353	MCF10A-Er-Src	breast:	n/a	chr7:12636253-12636261 chr7:12636252-12636262
26	FOS	chr7:12633814-12634095	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr7:12633791-12634114	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr7:12633801-12634084	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr7:12636142-12636299	MCF10A-Er-Src	breast:	n/a	chr7:12636253-12636261 chr7:12636252-12636262
30	FOXA1	chr7:12637008-12637176	T-47D	breast:	n/a	n/a
31	GATA2	chr7:12634846-12635195	K562	blood:	n/a	n/a
32	GATA3	chr7:12634743-12635204	MCF-7	breast:	n/a	chr7:12635038-12635046
33	GATA3	chr7:12634735-12635218	T-47D	breast:	n/a	chr7:12635038-12635046
34	GATA3	chr7:12634869-12635089	MCF-7	breast:	n/a	chr7:12635038-12635046
35	IRF1	chr7:12633937-12634311	K562	blood:	n/a	n/a
36	JUN	chr7:12642118-12642221	K562	blood:	n/a	n/a
37	JUND	chr7:12632342-12632400	K562	blood:	n/a	n/a
38	JUND	chr7:12633777-12634114	K562	blood:	n/a	n/a
39	JUND	chr7:12634901-12635215	K562	blood:	n/a	n/a
40	KAP1	chr7:12641778-12642345	K562	blood:	n/a	n/a
41	MAFF	chr7:12638681-12638848	HepG2	liver:	n/a	chr7:12638753-12638771
42	MAFK	chr7:12638683-12638915	HepG2	liver:	n/a	chr7:12638756-12638776
43	MAFK	chr7:12633935-12634000	K562	blood:	n/a	n/a
44	MAX	chr7:12634835-12635132	K562	blood:	n/a	n/a
45	MAX	chr7:12634908-12635058	K562	blood:	n/a	n/a
46	MAX	chr7:12634900-12635151	K562	blood:	n/a	n/a
47	MAZ	chr7:12633827-12634029	K562	blood:	n/a	n/a
48	MAZ	chr7:12634904-12635085	K562	blood:	n/a	n/a
49	MEF2A	chr7:12640941-12641239	GM12878	blood:	n/a	n/a
50	MYC	chr7:12634859-12635092	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12633679-12633729	RPTEC	kidney:	n/a
2	chr7:12633679-12633729	MCF10A-Er-Src	breast:	n/a
3	chr7:12633679-12633729	HepG2	liver:	n/a
4	chr7:12633679-12633729	AG09309	skin:	n/a
5	chr7:12633679-12633729	AG10803	skin:	n/a
6	chr7:12633679-12633729	CMK	blood:	n/a
7	chr7:12633679-12633729	K562	blood:	n/a
8	chr7:12633679-12633729	NHBE	bronchial:	n/a
9	chr7:12633679-12633729	SK-N-SH_RA	brain:	n/a
10	chr7:12633679-12633729	ProgFib	skin:	n/a
11	chr7:12633679-12633729	H1-hESC	embryonic stem cell:	embryo
12	chr7:12633679-12633729	GM12878	blood:	n/a
13	chr7:12633679-12633729	ovcar-3	ovarian:	n/a
14	chr7:12633679-12633729	U87	brain:	n/a
15	chr7:12633679-12633729	HAEpiC	amniotic membrane:	n/a
16	chr7:12633679-12633729	HEK293	kidney:	embryo
17	chr7:12633679-12633729	GM12891	blood:	n/a
18	chr7:12633679-12633729	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:12633679-12633729	HNPCEpiC	eye:	n/a
20	chr7:12633679-12633729	Hela-S3	cervix:	n/a
21	chr7:12633679-12633729	HMEC	breast:	n/a
22	chr7:12633679-12633729	AG09319	gingival:	n/a
23	chr7:12633679-12633729	SK-N-SH	brain:	n/a
24	chr7:12633679-12633729	HRE	kidney:	n/a
25	chr7:12633679-12633729	HCPEpiC	choroid plexus:	n/a
26	chr7:12633679-12633729	HRCEpiC	kidney:	n/a
27	chr7:12633679-12633729	Caco-2	colon:	n/a
28	chr7:12633679-12633729	PFSK-1	brain:	n/a
29	chr7:12633679-12633729	ECC-1	luminal epithelium:	n/a
30	chr7:12633679-12633729	AoSMC	blood vessel:	n/a
31	chr7:12633679-12633729	AG04449	skin:	fetal
32	chr7:12633679-12633729	NH-A	brain:	n/a
33	chr7:12633679-12633729	Jurkat	blood:	n/a
34	chr7:12633679-12633729	HEEpiC	esophagus:	n/a
35	chr7:12633679-12633729	IMR90	lung:	fetal
36	chr7:12633679-12633729	NB4	blood:	n/a
37	chr7:12633679-12633729	HIPEpiC	eye:	n/a
38	chr7:12633679-12633729	HCM	heart:	n/a
39	chr7:12633679-12633729	GM19239	blood:	n/a
40	chr7:12633679-12633729	T-47D	breast:	n/a
41	chr7:12633679-12633729	SKMC	muscle:	n/a
42	chr7:12633679-12633729	NT2-D1	testis:	n/a
43	chr7:12633679-12633729	Hepatocyte	liver:	n/a
44	chr7:12633679-12633729	HRPEpiC	eye:	n/a
45	chr7:12633679-12633729	MCF-7	breast:	n/a
46	chr7:12633679-12633729	BJ	skin:	n/a
47	chr7:12633679-12633729	HUVEC	blood vessel:	n/a
48	chr7:12633679-12633729	NHDF-neo	bronchial:	n/a
49	chr7:12633679-12633729	SK-N-MC	brain:	n/a
50	chr7:12633679-12633729	HCT-116	colon:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12632374..12633925-chr7:12635671..12637627,2	MCF-7	breast:
2	chr7:12639327..12643094-chr7:12646520..12649667,3	K562	blood:
3	chr7:12627909..12630200-chr7:12630367..12632328,2	MCF-7	breast:
4	chr7:12638001..12640706-chr7:12643352..12645469,2	K562	blood:
5	chr7:12632374..12633925-chr7:12635671..12637627,2	MCF-7	breast:
6	chr7:12628422..12631395-chr7:12632472..12635866,3	K562	blood:
7	chr7:12626568..12629559-chr7:12635307..12638295,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-VWDE-2	chr7:12632501-12632676	ENSG00000248523
2	lnc-VWDE-2	chr7:12634585-12634824	ENSG00000248523

No data

Variant related genes	Relation type
SCIN	TF binding region
SCIN	CpG island
ENSG00000006747	chromatin interactions
HMGA2	miRNA target sites

Extended variants
information (count: 603 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:603 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11764374	chr7:12632085-12632086	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544890481	chr7:12632104-12632105	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs142130699	chr7:12632124-12632125	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181265640	chr7:12632126-12632127	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs186087872	chr7:12632150-12632151	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs571713153	chr7:12632207-12632208	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs532221082	chr7:12632228-12632229	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs75466697	chr7:12632231-12632232	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs191042212	chr7:12632290-12632291	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs568684220	chr7:12632294-12632295	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs531406321	chr7:12632322-12632323	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs566670806	chr7:12632326-12632327	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs548040504	chr7:12632330-12632331	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568005034	chr7:12632341-12632342	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs75613968	chr7:12632351-12632352	Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs532349380	chr7:12632379-12632380	Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552186171	chr7:12632382-12632383	Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs566786250	chr7:12632397-12632398	Weak transcription Transcr. at gene 5' and 3' Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs190943120	chr7:12632466-12632467	Weak transcription Transcr. at gene 5' and 3' Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559114610	chr7:12632476-12632477	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs575858682	chr7:12632530-12632531	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
22	rs73678503	chr7:12632554-12632555	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
23	rs370644736	chr7:12632560-12632561	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
24	rs555251213	chr7:12632561-12632562	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
25	rs151166320	chr7:12632572-12632573	Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
26	rs540606341	chr7:12632620-12632621	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
27	rs560061577	chr7:12632634-12632635	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
28	rs183969672	chr7:12632654-12632655	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
29	rs538550204	chr7:12632683-12632684	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs554814765	chr7:12632720-12632721	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs545446554	chr7:12632734-12632735	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs562253275	chr7:12632751-12632752	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs186125542	chr7:12632752-12632753	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs547978753	chr7:12632759-12632760	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs1118998	chr7:12632767-12632768	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs1118999	chr7:12632774-12632775	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs370354387	chr7:12632799-12632800	Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs553085388	chr7:12632819-12632820	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs190540888	chr7:12632884-12632885	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs552660309	chr7:12632902-12632903	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182726268	chr7:12632918-12632919	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs187361883	chr7:12632920-12632921	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs137873370	chr7:12632940-12632941	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368112237	chr7:12632966-12632967	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs192790114	chr7:12632969-12632970	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs534480670	chr7:12632970-12632971	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs554173376	chr7:12632996-12632997	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149591643	chr7:12633013-12633014	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs576733770	chr7:12633015-12633016	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs545384292	chr7:12633028-12633029	Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
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
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12611800-12637600	Weak transcription	Colonic Mucosa	Colon
2	chr7:12625000-12645800	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:12625000-12652000	Weak transcription	Duodenum Mucosa	Duodenum
4	chr7:12625400-12667600	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr7:12625600-12633400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr7:12626200-12637400	Weak transcription	Pancreatic Islets	Pancreatic Islet
7	chr7:12627400-12633400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr7:12628000-12635600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr7:12631200-12632800	Transcr. at gene 5' and 3'	Placenta	Placenta
10	chr7:12632000-12632600	Enhancers	K562	blood
11	chr7:12632600-12632800	Flanking Active TSS	K562	blood
12	chr7:12632800-12633200	Active TSS	Placenta	Placenta
13	chr7:12632800-12633600	Active TSS	K562	blood
14	chr7:12633200-12633400	Transcr. at gene 5' and 3'	Placenta	Placenta
15	chr7:12633400-12635000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:12633400-12635000	ZNF genes & repeats	Placenta	Placenta
17	chr7:12633600-12634800	Flanking Active TSS	K562	blood
18	chr7:12633800-12634000	Enhancers	Esophagus	oesophagus
19	chr7:12634800-12635000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr7:12634800-12635600	Enhancers	K562	blood
21	chr7:12635000-12635600	Weak transcription	Placenta	Placenta
22	chr7:12635600-12636200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr7:12635600-12636200	Genic enhancers	K562	blood
24	chr7:12635600-12637200	Enhancers	Placenta	Placenta
25	chr7:12635800-12636200	Enhancers	Lung	lung
26	chr7:12636200-12637000	Enhancers	K562	blood
27	chr7:12636200-12638800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr7:12637000-12637200	Enhancers	Adipose Nuclei	Adipose
29	chr7:12637000-12644000	Weak transcription	K562	blood
30	chr7:12637200-12640200	Weak transcription	Placenta	Placenta
31	chr7:12637800-12638000	Enhancers	Adipose Nuclei	Adipose
32	chr7:12638800-12639000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr7:12639000-12639200	Genic enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr7:12639200-12639800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr7:12639800-12641400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:12639800-12649600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr7:12640200-12641400	Enhancers	GM12878-XiMat	blood
38	chr7:12641400-12644000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr7:12642400-12649200	Weak transcription	Pancreatic Islets	Pancreatic Islet
40	chr7:12642800-12649400	Weak transcription	Adipose Nuclei	Adipose
41	chr7:12644000-12644400	ZNF genes & repeats	K562	blood
42	chr7:12644000-12647000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr7:12644400-12649400	Weak transcription	K562	blood

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