Variant report

Variant	esv1831024
Chromosome Location	chr7:12964294-12974414
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:76)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:76 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr7:12969174-12969445	K562	blood:	n/a	n/a
2	ARID3A	chr7:12970216-12970508	K562	blood:	n/a	n/a
3	ATF1	chr7:12969223-12969475	K562	blood:	n/a	n/a
4	CEBPB	chr7:12970083-12970419	K562	blood:	n/a	n/a
5	CEBPB	chr7:12970127-12970424	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr7:12970093-12970407	K562	blood:	n/a	n/a
7	CEBPB	chr7:12970077-12970433	IMR90	lung:	n/a	n/a
8	CEBPB	chr7:12970154-12970363	K562	blood:	n/a	n/a
9	CEBPB	chr7:12970135-12970390	A549	lung:	n/a	n/a
10	CEBPD	chr7:12970210-12970566	K562	blood:	n/a	n/a
11	CTCF	chr7:12965740-12965890	HCM	heart:	n/a	n/a
12	EBF1	chr7:12969061-12969372	GM12878	blood:	n/a	chr7:12969215-12969224 chr7:12969214-12969224 chr7:12969213-12969224
13	EP300	chr7:12970228-12970461	Hela-S3	cervix:	n/a	n/a
14	EP300	chr7:12970275-12970671	K562	blood:	n/a	chr7:12970632-12970646
15	EP300	chr7:12967453-12967522	K562	blood:	n/a	n/a
16	EP300	chr7:12969253-12969794	K562	blood:	n/a	chr7:12969722-12969736
17	ESR1	chr7:12967784-12968008	T-47D	breast:	n/a	chr7:12967901-12967918
18	ESR1	chr7:12967662-12968051	ECC-1	luminal epithelium:	n/a	chr7:12967901-12967918
19	ESR1	chr7:12967793-12967976	ECC-1	luminal epithelium:	n/a	chr7:12967901-12967918
20	FOS	chr7:12970236-12970436	MCF10A-Er-Src	breast:	n/a	chr7:12970315-12970323
21	FOS	chr7:12970099-12970470	MCF10A-Er-Src	breast:	n/a	chr7:12970315-12970323
22	FOS	chr7:12970145-12970400	MCF10A-Er-Src	breast:	n/a	chr7:12970315-12970323
23	FOS	chr7:12963575-12964306	MCF10A-Er-Src	breast:	n/a	chr7:12964024-12964036
24	FOS	chr7:12970181-12970427	MCF10A-Er-Src	breast:	n/a	chr7:12970315-12970323
25	FOXA1	chr7:12972273-12972465	T-47D	breast:	n/a	n/a
26	GATA1	chr7:12967152-12968164	PBDE	blood:	n/a	n/a
27	GATA1	chr7:12969232-12969656	PBDE	blood:	n/a	chr7:12969281-12969289
28	GATA2	chr7:12970161-12970605	K562	blood:	n/a	n/a
29	GATA2	chr7:12970244-12970581	HUVEC	blood vessel:	n/a	n/a
30	GATA3	chr7:12970019-12970631	SK-N-SH	brain:	n/a	n/a
31	GATA3	chr7:12972299-12972537	MCF-7	breast:	n/a	n/a
32	GATA3	chr7:12970087-12970605	MCF-7	breast:	n/a	n/a
33	GATA3	chr7:12972193-12972560	T-47D	breast:	n/a	n/a
34	GATA3	chr7:12972374-12972410	SH-SY5Y	brain:	n/a	n/a
35	GATA3	chr7:12972217-12972509	T-47D	breast:	n/a	n/a
36	IRF1	chr7:12969361-12969527	K562	blood:	n/a	n/a
37	IRF1	chr7:12970364-12970644	K562	blood:	n/a	n/a
38	JUND	chr7:12970219-12970518	K562	blood:	n/a	chr7:12970315-12970323
39	JUND	chr7:12969203-12969552	K562	blood:	n/a	chr7:12969203-12969211
40	KAP1	chr7:12971917-12972047	K562	blood:	n/a	n/a
41	KAP1	chr7:12973774-12974085	K562	blood:	n/a	n/a
42	MAFK	chr7:12965916-12966050	HepG2	liver:	n/a	chr7:12966006-12966023
43	MAX	chr7:12971117-12971430	SK-N-SH	brain:	n/a	n/a
44	MXI1	chr7:12966263-12966304	H1-hESC	embryonic stem cell:	n/a	n/a
45	NR2F2	chr7:12965280-12965719	MCF-7	breast:	n/a	n/a
46	NR2F2	chr7:12965280-12965575	MCF-7	breast:	n/a	n/a
47	POLR2A	chr7:12965981-12966128	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr7:12967104-12967138	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr7:12971179-12971390	Gliobla	brain:	n/a	n/a
50	POLR2A	chr7:12970179-12970694	HUVEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:12971260-12971310	HCM	heart:	n/a
2	chr7:12971332-12971382	HCF	heart:	n/a
3	chr7:12971332-12971382	K562	blood:	n/a
4	chr7:12971332-12971382	BE2_C	brain:	n/a
5	chr7:12971332-12971382	SK-N-MC	brain:	n/a
6	chr7:12971260-12971310	Hela-S3	cervix:	n/a
7	chr7:12971260-12971310	LNCaP	prostate:	n/a
8	chr7:12971260-12971310	RPTEC	kidney:	n/a
9	chr7:12971332-12971382	HCPEpiC	choroid plexus:	n/a
10	chr7:12971332-12971382	H1-hESC	embryonic stem cell:	embryo
11	chr7:12971260-12971310	K562	blood:	n/a
12	chr7:12971332-12971382	AG09319	gingival:	n/a
13	chr7:12971332-12971382	HEEpiC	esophagus:	n/a
14	chr7:12971260-12971310	BJ	skin:	n/a
15	chr7:12971332-12971382	HRPEpiC	eye:	n/a
16	chr7:12971260-12971310	NHDF-neo	bronchial:	n/a
17	chr7:12971260-12971310	SK-N-SH_RA	brain:	n/a
18	chr7:12971260-12971310	GM06990	blood:	n/a
19	chr7:12971260-12971310	IMR90	lung:	fetal
20	chr7:12971332-12971382	SK-N-SH	brain:	n/a
21	chr7:12971260-12971310	GM12891	blood:	n/a
22	chr7:12971260-12971310	HAEpiC	amniotic membrane:	n/a
23	chr7:12971260-12971310	NHBE	bronchial:	n/a
24	chr7:12971260-12971310	GM19239	blood:	n/a
25	chr7:12971260-12971310	MCF-7	breast:	n/a
26	chr7:12971332-12971382	CMK	blood:	n/a
27	chr7:12971332-12971382	HRE	kidney:	n/a
28	chr7:12971260-12971310	H1-hESC	embryonic stem cell:	embryo
29	chr7:12971332-12971382	Caco-2	colon:	n/a
30	chr7:12971260-12971310	HEEpiC	esophagus:	n/a
31	chr7:12971332-12971382	ECC-1	luminal epithelium:	n/a
32	chr7:12971260-12971310	HRCEpiC	kidney:	n/a
33	chr7:12971332-12971382	AG04449	skin:	fetal
34	chr7:12971260-12971310	HNPCEpiC	eye:	n/a
35	chr7:12971332-12971382	GM12891	blood:	n/a
36	chr7:12971332-12971382	HUVEC	blood vessel:	n/a
37	chr7:12971332-12971382	PrEC	prostate:	n/a
38	chr7:12971260-12971310	ECC-1	luminal epithelium:	n/a
39	chr7:12971260-12971310	Caco-2	colon:	n/a
40	chr7:12971260-12971310	AoSMC	blood vessel:	n/a
41	chr7:12971260-12971310	AG09309	skin:	n/a
42	chr7:12971332-12971382	Hepatocyte	liver:	n/a
43	chr7:12971332-12971382	NHBE	bronchial:	n/a
44	chr7:12971260-12971310	Hepatocyte	liver:	n/a
45	chr7:12971332-12971382	T-47D	breast:	n/a
46	chr7:12971260-12971310	HIPEpiC	eye:	n/a
47	chr7:12971260-12971310	ovcar-3	ovarian:	n/a
48	chr7:12971332-12971382	RPTEC	kidney:	n/a
49	chr7:12971332-12971382	AoSMC	blood vessel:	n/a
50	chr7:12971260-12971310	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:12725420..12727462-chr7:12966302..12969517,3	MCF-7	breast:
2	chr7:12965459..12967674-chr7:12968950..12971042,2	K562	blood:
3	chr7:12915436..12917774-chr7:12964579..12966473,2	MCF-7	breast:
4	chr7:12965459..12967674-chr7:12968950..12971042,2	K562	blood:
5	chr7:12956747..12959826-chr7:12966112..12968954,4	K562	blood:
6	chr7:12753027..12755219-chr7:12963592..12965735,2	K562	blood:
7	chr7:12970290..12973079-chr7:13097205..13098974,2	K562	blood:

No data

Variant related genes	Relation type
RBMX2P4	TF binding region
RBMX2P4	CpG island
ENSG00000222974	chromatin interactions
ENSG00000122644	chromatin interactions

Extended variants
information (count: 427 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7804406	chr7:12964294-12964295	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs184071993	chr7:12964340-12964341	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs141115586	chr7:12964386-12964387	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs566038580	chr7:12964394-12964395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534916540	chr7:12964396-12964397	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs57768185	chr7:12964399-12964400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545985916	chr7:12964404-12964405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143977377	chr7:12964412-12964413	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376356095	chr7:12964430-12964431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs187561150	chr7:12964440-12964441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576263458	chr7:12964451-12964452	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556685958	chr7:12964469-12964470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190503936	chr7:12964560-12964561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs62448211	chr7:12964563-12964564	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559442875	chr7:12964618-12964619	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs528170786	chr7:12964629-12964630	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs545255502	chr7:12964635-12964636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs554875301	chr7:12964685-12964686	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs112303623	chr7:12964697-12964698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs530831746	chr7:12964779-12964780	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs555591835	chr7:12964811-12964812	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs117848844	chr7:12964837-12964838	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs13236466	chr7:12964850-12964851	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs573130854	chr7:12964851-12964852	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs376437603	chr7:12964882-12964883	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs549086000	chr7:12964904-12964905	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs42300	chr7:12964942-12964943	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs534761097	chr7:12964946-12964947	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs557950219	chr7:12964955-12964956	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs571459503	chr7:12964959-12964960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs182775332	chr7:12964974-12964975	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs557676486	chr7:12964998-12964999	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs574245859	chr7:12965024-12965025	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs34078	chr7:12965037-12965038	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs552676243	chr7:12965048-12965049	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572988266	chr7:12965068-12965069	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs533337875	chr7:12965082-12965083	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs34937649	chr7:12965085-12965086	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs144677697	chr7:12965101-12965102	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545936576	chr7:12965105-12965106	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138556757	chr7:12965106-12965107	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs544073589	chr7:12965107-12965108	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs561264015	chr7:12965108-12965109	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs148874569	chr7:12965125-12965126	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549374606	chr7:12965151-12965152	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370021060	chr7:12965152-12965153	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs529584603	chr7:12965200-12965201	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs143569920	chr7:12965230-12965231	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs368866233	chr7:12965231-12965232	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs34077	chr7:12965236-12965237	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:83)

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

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12961400-12964400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:12961400-12964400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr7:12962000-12967000	Weak transcription	Stomach Mucosa	stomach
4	chr7:12962000-12967400	Weak transcription	Fetal Intestine Large	intestine
5	chr7:12962000-12970200	Weak transcription	HUVEC	blood vessel
6	chr7:12962200-12967200	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr7:12962600-12966000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr7:12962800-12964400	Enhancers	HMEC	breast
9	chr7:12963000-12964400	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr7:12964200-12964800	Enhancers	NHEK	skin
11	chr7:12964200-12965200	Weak transcription	Liver	Liver
12	chr7:12964400-12965600	Weak transcription	HMEC	breast
13	chr7:12964400-12967200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr7:12964400-12969200	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:12964800-12965800	Weak transcription	NHEK	skin
16	chr7:12965200-12965600	Enhancers	Liver	Liver
17	chr7:12965200-12966600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr7:12965200-12966800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr7:12965200-12968200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:12965400-12966600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr7:12965400-12968400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr7:12965600-12966200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
23	chr7:12965800-12966000	Enhancers	HMEC	breast
24	chr7:12965800-12966200	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr7:12965800-12966200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr7:12965800-12966200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr7:12965800-12966200	Enhancers	NHEK	skin
28	chr7:12965800-12966400	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr7:12965800-12966400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr7:12966000-12966200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr7:12966000-12966200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr7:12966200-12967600	Weak transcription	NHEK	skin
33	chr7:12966200-12969200	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr7:12966400-12966800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr7:12966400-12967600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:12966400-12969200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr7:12966600-12967000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr7:12966600-12969200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr7:12966800-12968000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr7:12967000-12967400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr7:12967000-12969600	Enhancers	Stomach Mucosa	stomach
42	chr7:12967200-12967400	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr7:12967200-12968200	Enhancers	Ovary	ovary
44	chr7:12967200-12968200	Enhancers	Rectal Mucosa Donor 31	rectum
45	chr7:12967200-12968400	Enhancers	K562	blood
46	chr7:12967200-12969800	Enhancers	Fetal Intestine Small	intestine
47	chr7:12967400-12967600	Enhancers	Duodenum Mucosa	Duodenum
48	chr7:12967400-12967800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr7:12967400-12970200	Enhancers	Fetal Intestine Large	intestine
50	chr7:12967600-12968800	Weak transcription	Duodenum Mucosa	Duodenum

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