Variant report

Variant	esv3436157
Chromosome Location	chr11:16994276-16998574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:47)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:47 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr11:16996266-16996510	GM12878	blood:	n/a	n/a
2	CTCF	chr11:16994973-16995024	GM12878	blood:	n/a	n/a
3	CTCF	chr11:16996314-16996547	T-47D	breast:	n/a	n/a
4	CTCF	chr11:16994700-16994850	GM12873	blood:	n/a	chr11:16994828-16994836
5	E2F4	chr11:16997233-16997340	MCF10A-Er-Src	breast:	n/a	n/a
6	EBF1	chr11:16996237-16996531	GM12878	blood:	n/a	n/a
7	EP300	chr11:16996290-16996533	T-47D	breast:	n/a	n/a
8	FOSL2	chr11:16995848-16996044	HepG2	liver:	n/a	n/a
9	GATA2	chr11:16996167-16996567	K562	blood:	n/a	n/a
10	HEY1	chr11:16996276-16996634	K562	blood:	n/a	n/a
11	HEY1	chr11:16996329-16996674	HepG2	liver:	n/a	n/a
12	HEY1	chr11:16996352-16996622	K562	blood:	n/a	n/a
13	IRF4	chr11:16996247-16996588	GM12878	blood:	n/a	n/a
14	MAFF	chr11:16996867-16997144	HepG2	liver:	n/a	n/a
15	MAFK	chr11:16996909-16997123	HepG2	liver:	n/a	n/a
16	MAFK	chr11:16996839-16997146	HepG2	liver:	n/a	n/a
17	PAX5	chr11:16996354-16996570	GM12878	blood:	n/a	n/a
18	POLR2A	chr11:16998450-16998459	MCF-7	breast:	n/a	n/a
19	POLR2A	chr11:16996166-16996630	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr11:16996385-16996588	A549	lung:	n/a	n/a
21	POLR2A	chr11:16996134-16996646	GM12891	blood:	n/a	n/a
22	POLR2A	chr11:16996158-16996625	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr11:16996367-16996610	GM12891	blood:	n/a	n/a
24	POLR2A	chr11:16996197-16996640	GM12892	blood:	n/a	n/a
25	POLR2A	chr11:16996283-16996612	H1-hESC	embryonic stem cell:	n/a	n/a
26	POLR2A	chr11:16996201-16996650	GM12891	blood:	n/a	n/a
27	POLR2A	chr11:16996176-16996648	GM12892	blood:	n/a	n/a
28	POLR2A	chr11:16996408-16996618	A549	lung:	n/a	n/a
29	POLR2A	chr11:16996194-16996628	GM12891	blood:	n/a	n/a
30	POLR2A	chr11:16996142-16996203	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr11:16996153-16996608	Hela-S3	cervix:	n/a	n/a
32	POLR2A	chr11:16998522-16998531	MCF-7	breast:	n/a	n/a
33	POLR2A	chr11:16996220-16996624	GM12878	blood:	n/a	n/a
34	POLR2A	chr11:16996092-16996719	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:16996057-16996700	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr11:16996348-16996596	GM12878	blood:	n/a	n/a
37	POLR2A	chr11:16996136-16996643	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:16995076-16995095	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr11:16996405-16996582	A549	lung:	n/a	n/a
40	POLR2A	chr11:16996246-16996606	H1-hESC	embryonic stem cell:	n/a	n/a
41	POU2F2	chr11:16996145-16996649	GM12878	blood:	n/a	n/a
42	RFX5	chr11:16994801-16994874	HepG2	liver:	n/a	n/a
43	SIN3AK20	chr11:16996279-16996479	HepG2	liver:	n/a	n/a
44	SP1	chr11:16996284-16996588	H1-hESC	embryonic stem cell:	n/a	n/a
45	SPI1	chr11:16995346-16995473	K562	blood:	n/a	n/a
46	ZBTB33	chr11:16996270-16996513	GM12878	blood:	n/a	n/a
47	ZBTB33	chr11:16996187-16996739	K562	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:16998450-16998500	AG09309	skin:	n/a
2	chr11:16998450-16998500	K562	blood:	n/a
3	chr11:16998450-16998500	PFSK-1	brain:	n/a
4	chr11:16998450-16998500	AG04450	lung:	fetal
5	chr11:16998450-16998500	NHDF-neo	bronchial:	n/a
6	chr11:16998450-16998500	PrEC	prostate:	n/a
7	chr11:16998450-16998500	LNCaP	prostate:	n/a
8	chr11:16998450-16998500	SK-N-SH_RA	brain:	n/a
9	chr11:16998450-16998500	GM12892	blood:	n/a
10	chr11:16998450-16998500	HepG2	liver:	n/a
11	chr11:16998450-16998500	GM06990	blood:	n/a
12	chr11:16998450-16998500	Caco-2	colon:	n/a
13	chr11:16998450-16998500	A549	lung:	n/a
14	chr11:16998450-16998500	PANC-1	pancreas:	n/a
15	chr11:16998450-16998500	HAEpiC	amniotic membrane:	n/a
16	chr11:16998450-16998500	SAEC	small airway:	n/a
17	chr11:16998450-16998500	CMK	blood:	n/a
18	chr11:16998450-16998500	HCM	heart:	n/a
19	chr11:16998450-16998500	SKMC	muscle:	n/a
20	chr11:16998450-16998500	Hepatocyte	liver:	n/a
21	chr11:16998450-16998500	SK-N-MC	brain:	n/a
22	chr11:16998450-16998500	AoSMC	blood vessel:	n/a
23	chr11:16998450-16998500	NH-A	brain:	n/a
24	chr11:16998450-16998500	ProgFib	skin:	n/a
25	chr11:16998450-16998500	ovcar-3	ovarian:	n/a
26	chr11:16998450-16998500	HCPEpiC	choroid plexus:	n/a
27	chr11:16998450-16998500	NB4	blood:	n/a
28	chr11:16998450-16998500	AG10803	skin:	n/a
29	chr11:16998450-16998500	IMR90	lung:	fetal
30	chr11:16998450-16998500	AG04449	skin:	fetal
31	chr11:16998450-16998500	MCF-7	breast:	n/a
32	chr11:16998450-16998500	GM12878	blood:	n/a
33	chr11:16998450-16998500	SK-N-SH	brain:	n/a
34	chr11:16998450-16998500	HL-60	blood:	n/a
35	chr11:16998450-16998500	HMEC	breast:	n/a
36	chr11:16998450-16998500	Hela-S3	cervix:	n/a
37	chr11:16998450-16998500	BJ	skin:	n/a
38	chr11:16998450-16998500	HEEpiC	esophagus:	n/a
39	chr11:16998450-16998500	HIPEpiC	eye:	n/a
40	chr11:16998450-16998500	HRCEpiC	kidney:	n/a
41	chr11:16998450-16998500	HEK293	kidney:	embryo
42	chr11:16998450-16998500	U87	brain:	n/a
43	chr11:16998450-16998500	HRPEpiC	eye:	n/a
44	chr11:16998450-16998500	NHBE	bronchial:	n/a
45	chr11:16998450-16998500	HNPCEpiC	eye:	n/a
46	chr11:16998450-16998500	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:16998450-16998500	Jurkat	blood:	n/a
48	chr11:16998450-16998500	T-47D	breast:	n/a
49	chr11:16998450-16998500	RPTEC	kidney:	n/a
50	chr11:16998450-16998500	HCT-116	colon:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:16997842..17006545-chr11:17033236..17037894,15	MCF-7	breast:
2	chr11:16993487..16995936-chr11:17022091..17024047,2	MCF-7	breast:
3	chr11:16993725..16995475-chr11:17022309..17023867,2	MCF-7	breast:
4	chr11:16980989..16984063-chr11:16991605..16994714,3	MCF-7	breast:
5	chr11:16997178..16999092-chr11:17003135..17008712,4	MCF-7	breast:
6	chr11:16994632..16996478-chr11:17034698..17036230,2	MCF-7	breast:
7	chr11:16995340..16999228-chr11:17033547..17036418,3	MCF-7	breast:
8	chr11:16996626..17000145-chr11:17001852..17005291,4	K562	blood:

No data

Variant related genes	Relation type
RNU6-585P	TF binding region
ENSG00000244398	TF binding region
RNU6-585P	CpG island
ENSG00000244398	CpG island
ENSG00000166689	chromatin interactions
ENSG00000184669	chromatin interactions

Extended variants
information (count: 148 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:148 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs139280626	chr11:16994327-16994328	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs149590397	chr11:16994328-16994329	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs574265994	chr11:16994348-16994349	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs10741717	chr11:16994351-16994352	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs79371642	chr11:16994356-16994357	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs532724864	chr11:16994369-16994370	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs544718563	chr11:16994373-16994374	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs185838660	chr11:16994410-16994411	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs530646195	chr11:16994442-16994443	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549143452	chr11:16994443-16994444	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567487712	chr11:16994489-16994490	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115906398	chr11:16994491-16994492	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs370870708	chr11:16994503-16994504	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs7130301	chr11:16994581-16994582	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs566097430	chr11:16994582-16994583	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539816390	chr11:16994594-16994595	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs61881285	chr11:16994600-16994601	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs147235534	chr11:16994623-16994624	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs140735247	chr11:16994649-16994650	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs554879119	chr11:16994678-16994679	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs537287840	chr11:16994693-16994694	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs572293044	chr11:16994732-16994733	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs555925470	chr11:16994759-16994760	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs10832706	chr11:16994792-16994793	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs7116082	chr11:16994809-16994810	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs190164267	chr11:16994958-16994959	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs144646233	chr11:16995012-16995013	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs544581954	chr11:16995030-16995031	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs563075389	chr11:16995031-16995032	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115827748	chr11:16995034-16995035	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376356139	chr11:16995105-16995106	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs561137739	chr11:16995108-16995109	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs576356093	chr11:16995126-16995127	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs528241936	chr11:16995132-16995133	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs147952395	chr11:16995219-16995220	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs571546903	chr11:16995227-16995228	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs78671627	chr11:16995250-16995251	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs561944665	chr11:16995257-16995258	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs551790217	chr11:16995272-16995273	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs570210871	chr11:16995292-16995293	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs537557491	chr11:16995323-16995324	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs555539596	chr11:16995341-16995342	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs12291049	chr11:16995350-16995351	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs114459117	chr11:16995352-16995353	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs182489751	chr11:16995358-16995359	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs186765003	chr11:16995365-16995366	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs541147058	chr11:16995392-16995393	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs538285727	chr11:16995414-16995415	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs112968342	chr11:16995482-16995483	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs372515618	chr11:16995500-16995501	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Cancer	21183584	CNVD
Gastric adenocarcinoma	19115996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Thyroid cancer	19087340	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Wilms tumour	21544195	CNVD
Parathyroid adenoma	22454399	CNVD
Chordoma	21602918	CNVD
Breast cancer	21949216	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	19222835	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Beckwith-Wiedemann syndrome	21518781	CNVD
Wilms tumour	21518781	CNVD
Hepatoblastoma	21518781	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastric cancer	17908304	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Autism	22495311	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Multiple myeloma	16461302	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Lung adenocarcinoma	17086460	CNVD
Urothelial cell carcinoma	18451213	CNVD
Lung cancer	17086460	CNVD
Uterine serous papillary cancer	19536090	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:16981800-17002800	Weak transcription	Stomach Smooth Muscle	stomach
2	chr11:16982200-16999000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr11:16982200-17003800	Weak transcription	Right Ventricle	heart
4	chr11:16985200-16997600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr11:16985400-16997600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr11:16986800-16995000	Enhancers	Stomach Mucosa	stomach
7	chr11:16990000-16997400	Weak transcription	Lung	lung
8	chr11:16990000-16999000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:16990200-16998000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr11:16990200-16998000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr11:16990200-16999200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr11:16990800-16997400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:16991000-16994400	Weak transcription	Brain Substantia Nigra	brain
14	chr11:16991400-16998000	Weak transcription	Gastric	stomach
15	chr11:16991400-16999200	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr11:16991400-17002800	Weak transcription	Right Atrium	heart
17	chr11:16991600-16994600	Weak transcription	Brain Anterior Caudate	brain
18	chr11:16991600-16997400	Weak transcription	Brain Hippocampus Middle	brain
19	chr11:16991800-17001000	Weak transcription	Fetal Kidney	kidney
20	chr11:16991800-17001000	Weak transcription	HepG2	liver
21	chr11:16992000-16995000	Weak transcription	Pancreas	Pancrea
22	chr11:16992000-17001200	Weak transcription	Liver	Liver
23	chr11:16992200-17007400	Weak transcription	Colonic Mucosa	Colon
24	chr11:16992400-16998000	Weak transcription	Fetal Stomach	stomach
25	chr11:16992400-16998400	Weak transcription	Duodenum Mucosa	Duodenum
26	chr11:16992800-16999000	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr11:16993600-16995800	Strong transcription	Fetal Intestine Small	intestine
28	chr11:16993800-16998400	Weak transcription	Fetal Intestine Large	intestine
29	chr11:16993800-16999000	Weak transcription	Rectal Mucosa Donor 31	rectum
30	chr11:16994200-17000800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr11:16994400-16995200	Enhancers	Brain Substantia Nigra	brain
32	chr11:16994600-16995600	Enhancers	Brain Anterior Caudate	brain
33	chr11:16994600-16999400	Weak transcription	Placenta Amnion	Placenta Amnion
34	chr11:16994800-16995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:16994800-16995400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr11:16994800-16995600	Enhancers	Primary hematopoietic stem cells short term culture	blood
37	chr11:16995000-16995200	Enhancers	Pancreas	Pancrea
38	chr11:16995000-16998000	Weak transcription	Stomach Mucosa	stomach
39	chr11:16995200-16995400	Genic enhancers	Pancreas	Pancrea
40	chr11:16995200-16998200	Weak transcription	Brain Substantia Nigra	brain
41	chr11:16995400-16997600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr11:16995400-16997800	Weak transcription	Pancreas	Pancrea
43	chr11:16995600-16997600	Weak transcription	Brain Anterior Caudate	brain
44	chr11:16995800-16997400	Weak transcription	Fetal Intestine Small	intestine
45	chr11:16997400-16997600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr11:16997400-16997800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr11:16997400-16997800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr11:16997400-16998200	Enhancers	Lung	lung
49	chr11:16997400-16998800	Strong transcription	Fetal Intestine Small	intestine
50	chr11:16997400-17000000	Enhancers	Brain Hippocampus Middle	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links