Variant report

Variant	esv3378183
Chromosome Location	chr11:67264926-67267724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:39)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:39 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:67267219-67267263	Hela-S3	cervix:	n/a	n/a
2	POLR2A	chr11:67265578-67265739	ProgFib	skin:	n/a	n/a
3	POLR2A	chr11:67266300-67266631	K562	blood:	n/a	n/a
4	POLR2A	chr11:67267573-67267707	HepG2	liver:	n/a	n/a
5	POLR2A	chr11:67267344-67267419	K562	blood:	n/a	n/a
6	POLR2A	chr11:67267317-67267488	K562	blood:	n/a	n/a
7	POLR2A	chr11:67267571-67267944	K562	blood:	n/a	n/a
8	POLR2A	chr11:67267404-67268085	K562	blood:	n/a	n/a
9	POLR2A	chr11:67267182-67267765	HL-60	blood:	n/a	n/a
10	POLR2A	chr11:67265371-67265814	GM12878	blood:	n/a	n/a
11	POLR2A	chr11:67267689-67268153	K562	blood:	n/a	n/a
12	POLR2A	chr11:67267059-67268291	SK-N-MC	brain:	n/a	n/a
13	POLR2A	chr11:67265640-67265655	K562	blood:	n/a	n/a
14	POLR2A	chr11:67267512-67267533	K562	blood:	n/a	n/a
15	POLR2A	chr11:67267270-67268102	GM12878	blood:	n/a	n/a
16	POLR2A	chr11:67265968-67266531	SK-N-MC	brain:	n/a	n/a
17	POLR2A	chr11:67267084-67268162	A549	lung:	n/a	n/a
18	POLR2A	chr11:67266333-67266929	K562	blood:	n/a	n/a
19	POLR2A	chr11:67266136-67266292	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr11:67266261-67266282	K562	blood:	n/a	n/a
21	POLR2A	chr11:67267429-67267435	K562	blood:	n/a	n/a
22	POLR2A	chr11:67267542-67267560	HepG2	liver:	n/a	n/a
23	POLR2A	chr11:67266350-67266498	HepG2	liver:	n/a	n/a
24	POLR2A	chr11:67265570-67265618	HepG2	liver:	n/a	n/a
25	POLR2A	chr11:67265504-67265549	ProgFib	skin:	n/a	n/a
26	POLR2A	chr11:67266010-67266111	A549	lung:	n/a	n/a
27	POLR2A	chr11:67265363-67265840	GM12878	blood:	n/a	n/a
28	POLR2A	chr11:67266109-67266157	H1-hESC	embryonic stem cell:	n/a	n/a
29	POLR2A	chr11:67265652-67265806	Hela-S3	cervix:	n/a	n/a
30	POLR2A	chr11:67265295-67265348	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:67265235-67265347	K562	blood:	n/a	n/a
32	POLR2A	chr11:67266197-67266209	K562	blood:	n/a	n/a
33	POLR2A	chr11:67267453-67267483	K562	blood:	n/a	n/a
34	POLR2A	chr11:67265877-67266235	K562	blood:	n/a	n/a
35	POLR2A	chr11:67265699-67265955	K562	blood:	n/a	n/a
36	POLR2A	chr11:67266169-67266198	H1-hESC	embryonic stem cell:	n/a	n/a
37	POLR2A	chr11:67265644-67265670	HepG2	liver:	n/a	n/a
38	POLR2A	chr11:67267656-67268060	GM12878	blood:	n/a	n/a
39	STAT5A	chr11:67266317-67266873	GM12878	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:67266176-67266226	H1-hESC	embryonic stem cell:	embryo
2	chr11:67265369-67265419	HCPEpiC	choroid plexus:	n/a
3	chr11:67265369-67265419	AG09309	skin:	n/a
4	chr11:67265369-67265419	H1-hESC	embryonic stem cell:	embryo
5	chr11:67266089-67266139	H1-hESC	embryonic stem cell:	embryo
6	chr11:67266089-67266139	HIPEpiC	eye:	n/a
7	chr11:67266089-67266139	AG09319	gingival:	n/a
8	chr11:67265369-67265419	HUVEC	blood vessel:	n/a
9	chr11:67266176-67266226	AG10803	skin:	n/a
10	chr11:67266089-67266139	IMR90	lung:	fetal
11	chr11:67265369-67265419	AG04450	lung:	fetal
12	chr11:67266089-67266139	A549	lung:	n/a
13	chr11:67266089-67266139	ovcar-3	ovarian:	n/a
14	chr11:67265369-67265419	CMK	blood:	n/a
15	chr11:67266089-67266139	GM06990	blood:	n/a
16	chr11:67266128-67266178	HRPEpiC	eye:	n/a
17	chr11:67266128-67266178	GM06990	blood:	n/a
18	chr11:67265369-67265419	SK-N-SH	brain:	n/a
19	chr11:67265369-67265419	HRPEpiC	eye:	n/a
20	chr11:67265369-67265419	HAEpiC	amniotic membrane:	n/a
21	chr11:67265369-67265419	HCT-116	colon:	n/a
22	chr11:67266176-67266226	HRPEpiC	eye:	n/a
23	chr11:67265369-67265419	HCM	heart:	n/a
24	chr11:67266089-67266139	GM19239	blood:	n/a
25	chr11:67266176-67266226	HAEpiC	amniotic membrane:	n/a
26	chr11:67265369-67265419	HL-60	blood:	n/a
27	chr11:67265369-67265419	GM12892	blood:	n/a
28	chr11:67266089-67266139	CMK	blood:	n/a
29	chr11:67266176-67266226	ovcar-3	ovarian:	n/a
30	chr11:67265369-67265419	HepG2	liver:	n/a
31	chr11:67266128-67266178	AG09319	gingival:	n/a
32	chr11:67266176-67266226	BE2_C	brain:	n/a
33	chr11:67266089-67266139	AG04449	skin:	fetal
34	chr11:67266128-67266178	U87	brain:	n/a
35	chr11:67265369-67265419	GM06990	blood:	n/a
36	chr11:67265369-67265419	NHDF-neo	bronchial:	n/a
37	chr11:67266089-67266139	NH-A	brain:	n/a
38	chr11:67266176-67266226	AG04449	skin:	fetal
39	chr11:67266128-67266178	ECC-1	luminal epithelium:	n/a
40	chr11:67265369-67265419	NHBE	bronchial:	n/a
41	chr11:67266176-67266226	PrEC	prostate:	n/a
42	chr11:67266089-67266139	AG10803	skin:	n/a
43	chr11:67266176-67266226	HEK293	kidney:	embryo
44	chr11:67266176-67266226	SAEC	small airway:	n/a
45	chr11:67266089-67266139	HPAEpiC	pulmonary alveolar:	n/a
46	chr11:67266089-67266139	HCPEpiC	choroid plexus:	n/a
47	chr11:67266176-67266226	ECC-1	luminal epithelium:	n/a
48	chr11:67266089-67266139	SKMC	muscle:	n/a
49	chr11:67265369-67265419	HCF	heart:	n/a
50	chr11:67265369-67265419	NB4	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67263850..67266105-chr11:67266792..67269183,3	MCF-7	breast:
2	chr11:67263850..67266105-chr11:67266792..67269183,3	MCF-7	breast:
3	chr11:67249113..67250802-chr11:67267518..67269287,2	MCF-7	breast:
4	chr11:67161312..67163125-chr11:67265626..67268296,2	MCF-7	breast:
5	chr11:67201761..67204037-chr11:67264926..67266855,2	K562	blood:
6	chr11:67266460..67268680-chr11:67274631..67276596,2	MCF-7	breast:

No data

Variant related genes	Relation type
PITPNM1	TF binding region
PITPNM1	CpG island
ENSG00000110711	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000110697	chromatin interactions
ENSG00000253024	chromatin interactions
ENSG00000255949	chromatin interactions

Extended variants
information (count: 187 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:187 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201165712	chr11:67264938-67264939	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs377461389	chr11:67264956-67264957	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs199690826	chr11:67264972-67264973	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373996858	chr11:67265010-67265011	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547678982	chr11:67265011-67265012	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs139895981	chr11:67265042-67265043	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs367824069	chr11:67265067-67265068	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201803311	chr11:67265073-67265074	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs114575309	chr11:67265085-67265086	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146886366	chr11:67265086-67265087	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs139749051	chr11:67265094-67265095	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200633345	chr11:67265108-67265109	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372185175	chr11:67265112-67265113	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs376493442	chr11:67265113-67265114	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs144239455	chr11:67265118-67265119	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs532122322	chr11:67265134-67265135	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs202055588	chr11:67265141-67265142	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs201673089	chr11:67265158-67265159	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs369588837	chr11:67265164-67265165	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs147791085	chr11:67265197-67265198	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs542185377	chr11:67265217-67265218	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs554095298	chr11:67265264-67265265	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs572504192	chr11:67265281-67265282	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs376851934	chr11:67265291-67265292	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs531612516	chr11:67265306-67265307	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs117029606	chr11:67265335-67265336	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs531788098	chr11:67265354-67265355	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs543655539	chr11:67265355-67265356	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs111825548	chr11:67265356-67265357	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs373947707	chr11:67265368-67265369	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs376591979	chr11:67265377-67265378	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs376803073	chr11:67265385-67265386	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs149128402	chr11:67265398-67265399	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs370367742	chr11:67265413-67265414	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs143299011	chr11:67265420-67265421	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs151267105	chr11:67265427-67265428	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs201501265	chr11:67265428-67265429	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs566010672	chr11:67265429-67265430	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs527310668	chr11:67265430-67265431	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs78790481	chr11:67265444-67265445	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs570459164	chr11:67265463-67265464	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs202115767	chr11:67265492-67265493	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs191971089	chr11:67265498-67265499	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs374583205	chr11:67265512-67265513	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs568280910	chr11:67265535-67265536	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs201406420	chr11:67265537-67265538	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs148564747	chr11:67265539-67265540	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs371528353	chr11:67265563-67265564	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs572338358	chr11:67265582-67265583	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs565505996	chr11:67265597-67265598	Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Acute myeloid leukemia	21251322	CNVD
Lung cancer	19153074	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	22860045	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	21399695	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
small cell lung cancer	20016488	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:193 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67251000-67271000	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr11:67251400-67268000	Weak transcription	HSMMtube	muscle
3	chr11:67251400-67271200	Weak transcription	HSMM	muscle
4	chr11:67251400-67271400	Weak transcription	HUVEC	blood vessel
5	chr11:67251600-67268400	Weak transcription	NH-A	brain
6	chr11:67251600-67268600	Strong transcription	Fetal Intestine Small	intestine
7	chr11:67251600-67270600	Weak transcription	Fetal Heart	heart
8	chr11:67251600-67271400	Weak transcription	NHDF-Ad	bronchial
9	chr11:67252600-67270000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr11:67252600-67270200	Strong transcription	Fetal Stomach	stomach
11	chr11:67252600-67271600	Weak transcription	Psoas Muscle	Psoas
12	chr11:67252800-67270000	Weak transcription	Fetal Brain Male	brain
13	chr11:67252800-67271400	Weak transcription	Right Atrium	heart
14	chr11:67253800-67269600	Strong transcription	Cortex derived primary cultured neurospheres	brain
15	chr11:67254000-67265800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr11:67254000-67268000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
17	chr11:67254000-67268000	Strong transcription	Brain Germinal Matrix	brain
18	chr11:67254000-67268000	Strong transcription	Monocytes-CD14+_RO01746	blood
19	chr11:67254000-67270000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr11:67254000-67270800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:67254000-67271000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr11:67254200-67265600	Strong transcription	Lung	lung
23	chr11:67254200-67266400	Strong transcription	Brain Inferior Temporal Lobe	brain
24	chr11:67254200-67266400	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
25	chr11:67254200-67268600	Strong transcription	Gastric	stomach
26	chr11:67254400-67265000	Strong transcription	Liver	Liver
27	chr11:67254400-67268000	Strong transcription	Primary monocytes fromperipheralblood	blood
28	chr11:67254400-67268000	Strong transcription	Primary neutrophils fromperipheralblood	blood
29	chr11:67254400-67270600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr11:67254400-67271200	Weak transcription	K562	blood
31	chr11:67254600-67265800	Strong transcription	Adipose Nuclei	Adipose
32	chr11:67254600-67266000	Strong transcription	Left Ventricle	heart
33	chr11:67254600-67266800	Strong transcription	Primary T cells from cord blood	blood
34	chr11:67254600-67267000	Strong transcription	Fetal Brain Female	brain
35	chr11:67254600-67270600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
36	chr11:67254800-67265600	Strong transcription	Spleen	Spleen
37	chr11:67254800-67267400	Strong transcription	Thymus	Thymus
38	chr11:67254800-67270800	Strong transcription	Duodenum Mucosa	Duodenum
39	chr11:67254800-67271000	Weak transcription	HepG2	liver
40	chr11:67255000-67268000	Strong transcription	Placenta Amnion	Placenta Amnion
41	chr11:67255800-67270200	Strong transcription	Dnd41	blood
42	chr11:67255800-67272000	Weak transcription	Fetal Kidney	kidney
43	chr11:67256000-67270400	Strong transcription	Primary B cells from peripheral blood	blood
44	chr11:67256400-67270800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr11:67256600-67267000	Strong transcription	HUES6 Cell Line	embryonic stem cell
46	chr11:67256600-67270200	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr11:67256600-67270400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr11:67256600-67270600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
49	chr11:67257000-67270200	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:67257200-67266400	Strong transcription	Brain Cingulate Gyrus	brain

The 2.0 version of rSNPBase

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