Variant report

Variant	esv1801371
Chromosome Location	chr7:12498138-12522283
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:292)
CpG islands
(count:183)
Chromatin interactive
region (count:19)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:292 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12514982-12515589	K562	blood:	n/a	n/a
2	ARID3A	chr7:12513875-12513883	K562	blood:	n/a	n/a
3	ARID3A	chr7:12498199-12498492	K562	blood:	n/a	n/a
4	ARID3A	chr7:12498256-12498470	HepG2	liver:	n/a	n/a
5	ATF1	chr7:12514936-12515269	K562	blood:	n/a	n/a
6	BACH1	chr7:12514877-12514883	K562	blood:	n/a	n/a
7	BHLHE40	chr7:12514983-12515167	K562	blood:	n/a	n/a
8	BHLHE40	chr7:12521491-12521740	GM12878	blood:	n/a	n/a
9	CEBPB	chr7:12514893-12515314	K562	blood:	n/a	n/a
10	CEBPB	chr7:12514937-12515253	IMR90	lung:	n/a	n/a
11	CEBPB	chr7:12514886-12515412	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr7:12521403-12521540	H1-hESC	embryonic stem cell:	n/a	chr7:12521454-12521465
13	CEBPB	chr7:12514983-12515227	A549	lung:	n/a	n/a
14	CEBPB	chr7:12514581-12515394	K562	blood:	n/a	n/a
15	CEBPB	chr7:12519704-12519859	K562	blood:	n/a	n/a
16	CEBPB	chr7:12519662-12519793	A549	lung:	n/a	n/a
17	CEBPB	chr7:12521423-12521514	HepG2	liver:	n/a	chr7:12521454-12521465
18	CEBPB	chr7:12514935-12515135	HepG2	liver:	n/a	n/a
19	CTCF	chr7:12498260-12498410	HAc	cerebellar:	n/a	n/a
20	CTCF	chr7:12498189-12498488	Medullo	brain:	n/a	n/a
21	CTCF	chr7:12498260-12498410	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr7:12498240-12498390	HVMF	connective:	n/a	n/a
23	CTCF	chr7:12498260-12498410	HRPEpiC	eye:	n/a	n/a
24	CTCF	chr7:12498118-12498464	A549	lung:	n/a	n/a
25	CTCF	chr7:12498260-12498410	HPF	lung:	n/a	n/a
26	CTCF	chr7:12498450-12498465	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr7:12498240-12498390	HBMEC	blood vessel:	n/a	n/a
28	CTCF	chr7:12498260-12498410	AG04450	lung:	n/a	n/a
29	CTCF	chr7:12498260-12498410	GM12864	blood:	n/a	n/a
30	CTCF	chr7:12498140-12498561	MCF-7	breast:	n/a	n/a
31	CTCF	chr7:12498280-12498430	HRPEpiC	eye:	n/a	n/a
32	CTCF	chr7:12498218-12498459	GM13977	blood:	n/a	n/a
33	CTCF	chr7:12498280-12498430	HPF	lung:	n/a	n/a
34	CTCF	chr7:12498220-12498370	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr7:12498135-12498524	HepG2	liver:	n/a	n/a
36	CTCF	chr7:12498300-12498450	GM12872	blood:	n/a	n/a
37	CTCF	chr7:12501098-12501132	GM10248	blood:	n/a	n/a
38	CTCF	chr7:12498540-12498690	Caco-2	colon:	n/a	n/a
39	CTCF	chr7:12498198-12498485	GM12878	blood:	n/a	n/a
40	CTCF	chr7:12498260-12498410	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr7:12498190-12498456	A549	lung:	n/a	n/a
42	CTCF	chr7:12498240-12498390	GM12867	blood:	n/a	n/a
43	CTCF	chr7:12498260-12498410	BE2_C	brain:	n/a	n/a
44	CTCF	chr7:12498280-12498430	GM12866	blood:	n/a	n/a
45	CTCF	chr7:12498200-12498350	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr7:12498240-12498390	GM12872	blood:	n/a	n/a
47	CTCF	chr7:12498280-12498430	MCF-7	breast:	n/a	n/a
48	CTCF	chr7:12498173-12498418	A549	lung:	n/a	n/a
49	CTCF	chr7:12498260-12498410	GM12866	blood:	n/a	n/a
50	CTCF	chr7:12498240-12498390	GM12868	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12510772-12510822	BE2_C	brain:	n/a
2	chr7:12510772-12510822	GM12891	blood:	n/a
3	chr7:12510665-12510715	NHDF-neo	bronchial:	n/a
4	chr7:12510772-12510822	HMEC	breast:	n/a
5	chr7:12510665-12510715	T-47D	breast:	n/a
6	chr7:12510863-12510913	AG10803	skin:	n/a
7	chr7:12510863-12510913	NH-A	brain:	n/a
8	chr7:12510863-12510913	HRPEpiC	eye:	n/a
9	chr7:12510772-12510822	Caco-2	colon:	n/a
10	chr7:12510665-12510715	PrEC	prostate:	n/a
11	chr7:12510863-12510913	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:12510863-12510913	Hepatocyte	liver:	n/a
13	chr7:12510863-12510913	AG04450	lung:	fetal
14	chr7:12510665-12510715	HEEpiC	esophagus:	n/a
15	chr7:12510665-12510715	K562	blood:	n/a
16	chr7:12510863-12510913	NB4	blood:	n/a
17	chr7:12510665-12510715	AG04450	lung:	fetal
18	chr7:12510772-12510822	GM12892	blood:	n/a
19	chr7:12510772-12510822	U87	brain:	n/a
20	chr7:12510665-12510715	HCF	heart:	n/a
21	chr7:12510772-12510822	HL-60	blood:	n/a
22	chr7:12510863-12510913	ProgFib	skin:	n/a
23	chr7:12510665-12510715	GM12891	blood:	n/a
24	chr7:12510772-12510822	AG09319	gingival:	n/a
25	chr7:12510665-12510715	BJ	skin:	n/a
26	chr7:12510772-12510822	HCPEpiC	choroid plexus:	n/a
27	chr7:12510863-12510913	SKMC	muscle:	n/a
28	chr7:12510665-12510715	HepG2	liver:	n/a
29	chr7:12510772-12510822	SK-N-MC	brain:	n/a
30	chr7:12510665-12510715	HIPEpiC	eye:	n/a
31	chr7:12510665-12510715	HCM	heart:	n/a
32	chr7:12510772-12510822	HCT-116	colon:	n/a
33	chr7:12510863-12510913	H1-hESC	embryonic stem cell:	embryo
34	chr7:12510863-12510913	HCM	heart:	n/a
35	chr7:12510863-12510913	MCF-7	breast:	n/a
36	chr7:12510772-12510822	MCF-7	breast:	n/a
37	chr7:12510665-12510715	HRE	kidney:	n/a
38	chr7:12510665-12510715	HNPCEpiC	eye:	n/a
39	chr7:12510665-12510715	ProgFib	skin:	n/a
40	chr7:12510863-12510913	PANC-1	pancreas:	n/a
41	chr7:12510772-12510822	HUVEC	blood vessel:	n/a
42	chr7:12510665-12510715	AG09319	gingival:	n/a
43	chr7:12510863-12510913	MCF10A-Er-Src	breast:	n/a
44	chr7:12510863-12510913	HCT-116	colon:	n/a
45	chr7:12510863-12510913	HUVEC	blood vessel:	n/a
46	chr7:12510772-12510822	NT2-D1	testis:	n/a
47	chr7:12510863-12510913	HepG2	liver:	n/a
48	chr7:12510863-12510913	HRCEpiC	kidney:	n/a
49	chr7:12510863-12510913	CMK	blood:	n/a
50	chr7:12510772-12510822	SK-N-SH_RA	brain:	n/a

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
2	chr7:12520796..12522779-chr7:12527850..12529893,2	K562	blood:
3	chr7:12497831..12498808-chr7:12529325..12530426,5	K562	blood:
4	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:
5	chr7:12498003..12498630-chr7:12536129..12537096,2	K562	blood:
6	chr7:12438246..12440772-chr7:12512038..12514677,2	K562	blood:
7	chr7:12496465..12498567-chr7:12529648..12531435,2	K562	blood:
8	chr7:12485193..12487796-chr7:12515501..12517755,2	K562	blood:
9	chr7:12497870..12498820-chr7:12528972..12530631,10	MCF-7	breast:
10	chr7:12516830..12519772-chr7:12523106..12525607,3	K562	blood:
11	chr7:12511799..12515284-chr7:12517629..12521714,3	K562	blood:
12	chr7:12488598..12490554-chr7:12506071..12508415,2	K562	blood:
13	chr7:12497629..12498696-chr7:12535919..12536815,4	MCF-7	breast:
14	chr7:12497885..12498702-chr7:12558562..12559343,2	MCF-7	breast:
15	chr7:12497882..12499037-chr7:12533987..12535337,10	MCF-7	breast:
16	chr7:11466869..11467685-chr7:12498254..12498786,2	MCF-7	breast:
17	chr7:12497991..12498705-chr7:12529442..12530188,2	MCF-7	breast:
18	chr7:12497632..12498790-chr7:12662958..12664405,3	K562	blood:
19	chr7:12511799..12514210-chr7:12517629..12520508,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000236048	TF binding region
ENSG00000236048	CpG island
ENSG00000226690	chromatin interactions
ENSG00000203523	chromatin interactions

Extended variants
information (count: 941 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12669338	chr7:12498138-12498139	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs367786442	chr7:12498147-12498148	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs75991360	chr7:12498176-12498177	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs529978945	chr7:12498179-12498180	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546889518	chr7:12498199-12498200	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559989933	chr7:12498227-12498228	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs112247085	chr7:12498235-12498236	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs568072899	chr7:12498260-12498261	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs551914623	chr7:12498273-12498274	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs568654852	chr7:12498275-12498276	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs145850615	chr7:12498284-12498285	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs533455513	chr7:12498311-12498312	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs180820920	chr7:12498341-12498342	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs546843566	chr7:12498348-12498349	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs848030	chr7:12498432-12498433	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554508066	chr7:12498439-12498440	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs577571753	chr7:12498462-12498463	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs187294837	chr7:12498467-12498468	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs12667501	chr7:12498511-12498512	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs539727807	chr7:12498518-12498519	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs142922267	chr7:12498537-12498538	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs848029	chr7:12498539-12498540	Inactive region	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs562006176	chr7:12498549-12498550	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs572427993	chr7:12498554-12498555	Inactive region	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs551272158	chr7:12498595-12498596	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192137857	chr7:12498613-12498614	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs532267558	chr7:12498631-12498632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs12699374	chr7:12498634-12498635	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs562326633	chr7:12498637-12498638	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs576817782	chr7:12498645-12498646	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs531367124	chr7:12498671-12498672	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs12699375	chr7:12498686-12498687	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs568016797	chr7:12498687-12498688	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555321424	chr7:12504027-12504028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs368125942	chr7:12504037-12504038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs565649377	chr7:12504040-12504041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574427030	chr7:12504048-12504049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs373667030	chr7:12504121-12504122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs574102585	chr7:12504126-12504127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7801555	chr7:12504151-12504152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs28862396	chr7:12504168-12504169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs143727470	chr7:12504255-12504256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs138371578	chr7:12504278-12504279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551158038	chr7:12504300-12504301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369849189	chr7:12504327-12504328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545641389	chr7:12504329-12504330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562647189	chr7:12504339-12504340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs848024	chr7:12504372-12504373	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs192200689	chr7:12504385-12504386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184210695	chr7:12504399-12504400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:51 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12504000-12510600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr7:12508800-12509200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr7:12510600-12510800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr7:12510800-12515000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr7:12513400-12514000	Enhancers	K562	blood
6	chr7:12513600-12514200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
7	chr7:12513600-12516200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr7:12514000-12515000	Weak transcription	K562	blood
9	chr7:12514200-12515200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:12514600-12516000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr7:12515000-12515200	Enhancers	K562	blood
12	chr7:12515000-12515400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
13	chr7:12515000-12515600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr7:12515000-12515600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:12515000-12515600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr7:12515000-12515600	Enhancers	Fetal Heart	heart
17	chr7:12515000-12515600	Enhancers	Ovary	ovary
18	chr7:12515000-12515600	Enhancers	NH-A	brain
19	chr7:12515000-12515600	Enhancers	Osteobl	bone
20	chr7:12515000-12515800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr7:12515000-12515800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr7:12515200-12515400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:12515200-12515600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr7:12515200-12515600	Enhancers	Muscle Satellite Cultured Cells	--
25	chr7:12515200-12515600	Enhancers	Hela-S3	cervix
26	chr7:12515200-12515600	Flanking Active TSS	K562	blood
27	chr7:12515200-12515800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr7:12515200-12515800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:12515200-12516000	Enhancers	Fetal Lung	lung
30	chr7:12515400-12515600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr7:12515400-12515800	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr7:12515400-12515800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr7:12515400-12516000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr7:12515600-12516000	Enhancers	K562	blood
35	chr7:12515600-12521000	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr7:12521000-12521400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr7:12521000-12521600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr7:12521000-12521600	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
39	chr7:12521000-12521800	Enhancers	Primary T cells from cord blood	blood
40	chr7:12521000-12522400	Enhancers	GM12878-XiMat	blood
41	chr7:12521200-12521400	Enhancers	Primary T helper cells fromperipheralblood	blood
42	chr7:12521400-12521800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr7:12521400-12521800	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr7:12521400-12521800	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
45	chr7:12521400-12522000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
46	chr7:12521400-12522400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
47	chr7:12521600-12521800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:12521600-12522000	Enhancers	Primary T helper cells PMA-I stimulated	--
49	chr7:12521800-12522000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr7:12521800-12522000	Enhancers	Primary T helper cells fromperipheralblood	blood

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