Variant report

Variant	esv3362683
Chromosome Location	chr11:64517876-64521874
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr11:64519031-64519387	K562	blood:	n/a	n/a
2	CBX3	chr11:64519075-64519394	K562	blood:	n/a	n/a
3	CEBPB	chr11:64519145-64519490	HepG2	liver:	n/a	chr11:64519322-64519333
4	CEBPB	chr11:64519271-64519343	IMR90	lung:	n/a	chr11:64519322-64519333
5	CEBPB	chr11:64519150-64519480	HepG2	liver:	n/a	chr11:64519322-64519333
6	CEBPB	chr11:64519228-64519409	K562	blood:	n/a	chr11:64519322-64519333
7	CTCF	chr11:64518299-64518321	Kidney_OC	kidney:	n/a	n/a
8	CTCF	chr11:64518220-64518404	Spleen_OC	spleen:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
9	CTCF	chr11:64518160-64518310	HCM	heart:	n/a	n/a
10	CTCF	chr11:64518229-64518402	MCF-7	breast:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
11	CTCF	chr11:64518240-64518390	HFF	foreskin:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
12	CTCF	chr11:64518220-64518370	A549	lung:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
13	CTCF	chr11:64518200-64518350	SAEC	small airway:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
14	CTCF	chr11:64518180-64518330	NB4	blood:	n/a	n/a
15	CTCF	chr11:64518260-64518410	HFF-Myc	foreskin:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
16	CTCF	chr11:64518260-64518410	HAc	cerebellar:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
17	CTCF	chr11:64518240-64518390	HCT-116	colon:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
18	CTCF	chr11:64518265-64518320	GM12892	blood:	n/a	n/a
19	CTCF	chr11:64518265-64518326	GM19239	blood:	n/a	n/a
20	CTCF	chr11:64518260-64518410	HVMF	connective:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
21	CTCF	chr11:64518200-64518350	HepG2	liver:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
22	CTCF	chr11:64518200-64518350	HMF	breast:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
23	CTCF	chr11:64518160-64518310	AG04450	lung:	n/a	n/a
24	CTCF	chr11:64518220-64518370	HRE	kidney:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
25	CTCF	chr11:64518200-64518350	GM12875	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
26	CTCF	chr11:64518180-64518330	HAc	cerebellar:	n/a	n/a
27	CTCF	chr11:64518240-64518390	A549	lung:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
28	CTCF	chr11:64518240-64518390	GM12864	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
29	CTCF	chr11:64518220-64518370	HBMEC	blood vessel:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
30	CTCF	chr11:64518200-64518350	HA-sp	spinal cord:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
31	CTCF	chr11:64518240-64518390	HCPEpiC	choroid plexus:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
32	CTCF	chr11:64518211-64518408	GM12878	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
33	CTCF	chr11:64518180-64518330	GM06990	blood:	n/a	n/a
34	CTCF	chr11:64518260-64518410	RPTEC	kidney:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
35	CTCF	chr11:64518240-64518390	HEK293	kidney:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
36	CTCF	chr11:64518220-64518370	GM12864	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
37	CTCF	chr11:64518200-64518350	WERI-Rb-1	eye:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
38	CTCF	chr11:64518200-64518350	HMEC	breast:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
39	CTCF	chr11:64518149-64518422	H1-hESC	embryonic stem cell:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
40	CTCF	chr11:64518100-64518250	GM06990	blood:	n/a	n/a
41	CTCF	chr11:64521740-64521890	HEK293	kidney:	n/a	n/a
42	CTCF	chr11:64518200-64518350	Hela-S3	cervix:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
43	CTCF	chr11:64518200-64518350	HCPEpiC	choroid plexus:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
44	CTCF	chr11:64518220-64518370	HPAF	blood vessel:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
45	CTCF	chr11:64518200-64518350	GM12878	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
46	CTCF	chr11:64518220-64518370	SK-N-SH_RA	brain:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
47	CTCF	chr11:64518240-64518390	GM12874	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
48	CTCF	chr11:64518246-64518376	MCF-7	breast:	n/a	chr11:64518324-64518345 chr11:64518323-64518339
49	CTCF	chr11:64517980-64518130	A549	lung:	n/a	n/a
50	CTCF	chr11:64518220-64518370	K562	blood:	n/a	chr11:64518324-64518345 chr11:64518323-64518339

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:64521052-64521102	T-47D	breast:	n/a
2	chr11:64521052-64521102	ECC-1	luminal epithelium:	n/a
3	chr11:64521052-64521102	RPTEC	kidney:	n/a
4	chr11:64521142-64521192	HCF	heart:	n/a
5	chr11:64521052-64521102	HCT-116	colon:	n/a
6	chr11:64521052-64521102	SAEC	small airway:	n/a
7	chr11:64521142-64521192	AoSMC	blood vessel:	n/a
8	chr11:64521052-64521102	ProgFib	skin:	n/a
9	chr11:64521088-64521138	SK-N-SH_RA	brain:	n/a
10	chr11:64521088-64521138	A549	lung:	n/a
11	chr11:64521052-64521102	AG04450	lung:	fetal
12	chr11:64521142-64521192	GM12891	blood:	n/a
13	chr11:64521052-64521102	GM12878	blood:	n/a
14	chr11:64521142-64521192	ProgFib	skin:	n/a
15	chr11:64521142-64521192	SK-N-SH	brain:	n/a
16	chr11:64521088-64521138	HAEpiC	amniotic membrane:	n/a
17	chr11:64521052-64521102	PANC-1	pancreas:	n/a
18	chr11:64521088-64521138	MCF10A-Er-Src	breast:	n/a
19	chr11:64521142-64521192	RPTEC	kidney:	n/a
20	chr11:64521088-64521138	BE2_C	brain:	n/a
21	chr11:64521142-64521192	SAEC	small airway:	n/a
22	chr11:64521142-64521192	HRPEpiC	eye:	n/a
23	chr11:64521088-64521138	K562	blood:	n/a
24	chr11:64521052-64521102	HAEpiC	amniotic membrane:	n/a
25	chr11:64521142-64521192	CMK	blood:	n/a
26	chr11:64521088-64521138	HEEpiC	esophagus:	n/a
27	chr11:64521052-64521102	H1-hESC	embryonic stem cell:	embryo
28	chr11:64521052-64521102	NB4	blood:	n/a
29	chr11:64521088-64521138	HNPCEpiC	eye:	n/a
30	chr11:64521088-64521138	HRCEpiC	kidney:	n/a
31	chr11:64521088-64521138	NHDF-neo	bronchial:	n/a
32	chr11:64521088-64521138	U87	brain:	n/a
33	chr11:64521142-64521192	SKMC	muscle:	n/a
34	chr11:64521088-64521138	SK-N-MC	brain:	n/a
35	chr11:64521052-64521102	NT2-D1	testis:	n/a
36	chr11:64521088-64521138	NH-A	brain:	n/a
37	chr11:64521088-64521138	T-47D	breast:	n/a
38	chr11:64521142-64521192	AG04450	lung:	fetal
39	chr11:64521088-64521138	CMK	blood:	n/a
40	chr11:64521088-64521138	RPTEC	kidney:	n/a
41	chr11:64521142-64521192	NB4	blood:	n/a
42	chr11:64521142-64521192	GM12878	blood:	n/a
43	chr11:64521052-64521102	HEEpiC	esophagus:	n/a
44	chr11:64521142-64521192	U87	brain:	n/a
45	chr11:64521088-64521138	Hepatocyte	liver:	n/a
46	chr11:64521052-64521102	NHBE	bronchial:	n/a
47	chr11:64521088-64521138	SKMC	muscle:	n/a
48	chr11:64521052-64521102	A549	lung:	n/a
49	chr11:64521142-64521192	HRE	kidney:	n/a
50	chr11:64521088-64521138	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr11:64514464..64517911-chr11:64519413..64523331,4	MCF-7	breast:
2	chr11:64514464..64517911-chr11:64519413..64523331,4	MCF-7	breast:
3	chr11:64508515..64511238-chr11:64521497..64525046,4	MCF-7	breast:

Variant related genes	Relation type
RASGRP2	TF binding region
PYGM	TF binding region
RASGRP2	CpG island
PYGM	CpG island
ENSG00000068831	chromatin interactions
ENSG00000068976	chromatin interactions

Extended variants
information (count: 233 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:233 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370880123	chr11:64517905-64517906	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs61737361	chr11:64517913-64517914	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs200537357	chr11:64517916-64517917	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs147725917	chr11:64517940-64517941	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs200688234	chr11:64517947-64517948	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs140349323	chr11:64517956-64517957	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs144081869	chr11:64517969-64517970	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs372078244	chr11:64517994-64517995	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs2230309	chr11:64517999-64518000	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs113806080	chr11:64518016-64518017	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs119103256	chr11:64518029-64518030	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs111748191	chr11:64518058-64518059	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs537230893	chr11:64518074-64518075	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs199633469	chr11:64518098-64518099	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs532168943	chr11:64518126-64518127	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs552165335	chr11:64518131-64518132	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs568256371	chr11:64518156-64518157	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs528264823	chr11:64518178-64518179	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs547942876	chr11:64518247-64518248	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs190627991	chr11:64518249-64518250	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs75024721	chr11:64518345-64518346	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs540292189	chr11:64518366-64518367	Weak transcription Genic enhancers Strong transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs556256784	chr11:64518420-64518421	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs569932955	chr11:64518423-64518424	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs182444263	chr11:64518425-64518426	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558981977	chr11:64518432-64518433	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs187182392	chr11:64518433-64518434	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs71583721	chr11:64518504-64518505	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs592546	chr11:64518511-64518512	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs592532	chr11:64518517-64518518	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs2071320	chr11:64518520-64518521	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs567015840	chr11:64518521-64518522	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs592521	chr11:64518525-64518526	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs558947384	chr11:64518529-64518530	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111543138	chr11:64518530-64518531	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs58190568	chr11:64518531-64518532	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs545824778	chr11:64518543-64518544	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs569138464	chr11:64518583-64518584	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111801074	chr11:64518645-64518646	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs559097797	chr11:64518729-64518730	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs34195091	chr11:64518791-64518792	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs372377149	chr11:64518793-64518794	Weak transcription Enhancers Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs119103253	chr11:64518803-64518804	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs368964406	chr11:64518804-64518805	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
45	rs61736659	chr11:64518809-64518810	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
46	rs114073621	chr11:64518818-64518819	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
47	rs150098198	chr11:64518841-64518842	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
48	rs116180923	chr11:64518842-64518843	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
49	rs141267088	chr11:64518847-64518848	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
50	rs368385152	chr11:64518862-64518863	Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	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
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	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
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	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
Chronic lymphocytic leukemia	22228453	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64512800-64526400	Weak transcription	Ovary	ovary
2	chr11:64513400-64529800	Weak transcription	Liver	Liver
3	chr11:64513400-64530000	Weak transcription	Aorta	Aorta
4	chr11:64513600-64518800	Weak transcription	Brain Substantia Nigra	brain
5	chr11:64513600-64518800	Weak transcription	Duodenum Smooth Muscle	Duodenum
6	chr11:64513600-64518800	Weak transcription	Left Ventricle	heart
7	chr11:64513600-64522200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:64513600-64525600	Weak transcription	Psoas Muscle	Psoas
9	chr11:64513600-64526200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr11:64513600-64526200	Weak transcription	Esophagus	oesophagus
11	chr11:64513800-64519200	Weak transcription	Brain Anterior Caudate	brain
12	chr11:64513800-64526400	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr11:64513800-64526800	Weak transcription	Brain Hippocampus Middle	brain
14	chr11:64513800-64526800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr11:64514000-64518800	Weak transcription	Lung	lung
16	chr11:64514000-64518800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr11:64514000-64521000	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr11:64514000-64526800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr11:64514000-64529800	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr11:64514200-64518000	Weak transcription	Primary neutrophils fromperipheralblood	blood
21	chr11:64514200-64518000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr11:64514200-64518000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
23	chr11:64514200-64519000	Weak transcription	Gastric	stomach
24	chr11:64514200-64519200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
25	chr11:64514200-64522400	Weak transcription	Fetal Heart	heart
26	chr11:64514400-64518600	Weak transcription	Spleen	Spleen
27	chr11:64514400-64526600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chr11:64514600-64529800	Weak transcription	Dnd41	blood
29	chr11:64515000-64518000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr11:64515200-64526000	Weak transcription	Placenta Amnion	Placenta Amnion
31	chr11:64515200-64527600	Weak transcription	Primary hematopoietic stem cells	blood
32	chr11:64515400-64518000	Enhancers	Primary B cells from peripheral blood	blood
33	chr11:64515800-64518000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr11:64515800-64518600	Weak transcription	Placenta	Placenta
35	chr11:64515800-64518600	Weak transcription	Fetal Thymus	thymus
36	chr11:64515800-64519800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr11:64515800-64526400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr11:64516000-64527400	Weak transcription	Fetal Intestine Small	intestine
39	chr11:64516000-64529800	Weak transcription	Fetal Brain Female	brain
40	chr11:64516200-64518200	Enhancers	Primary B cells from cord blood	blood
41	chr11:64517200-64519600	Strong transcription	Fetal Muscle Leg	muscle
42	chr11:64517600-64518000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr11:64517600-64518400	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr11:64517600-64518800	Genic enhancers	Skeletal Muscle Male	skeletal muscle
45	chr11:64517600-64519000	Genic enhancers	Primary T cells from cord blood	blood
46	chr11:64517600-64519000	Genic enhancers	Primary T helper cells PMA-I stimulated	--
47	chr11:64517600-64519000	Genic enhancers	Primary T helper cells fromperipheralblood	blood
48	chr11:64517600-64519000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr11:64517600-64520000	Strong transcription	Fetal Muscle Trunk	muscle
50	chr11:64517600-64520000	Strong transcription	Fetal Stomach	stomach

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