Variant report

Variant	esv1010387
Chromosome Location	chr11:67163827-67164654
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:80)
CpG islands
(count:0)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:80 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:67164482-67164775	GM12878	blood:	n/a	n/a
2	ELF1	chr11:67163931-67164820	GM12878	blood:	n/a	chr11:67164124-67164136
3	ELF1	chr11:67164305-67164655	K562	blood:	n/a	n/a
4	MTA3	chr11:67163641-67165543	GM12878	blood:	n/a	n/a
5	NFATC1	chr11:67164126-67164407	GM12878	blood:	n/a	n/a
6	POLR2A	chr11:67162822-67167423	K562	blood:	n/a	n/a
7	POLR2A	chr11:67162576-67164718	U87	brain:	n/a	n/a
8	POLR2A	chr11:67164061-67164307	Hela-S3	cervix:	n/a	n/a
9	POLR2A	chr11:67163894-67164118	ProgFib	skin:	n/a	n/a
10	POLR2A	chr11:67163762-67167367	K562	blood:	n/a	n/a
11	POLR2A	chr11:67164110-67164126	HepG2	liver:	n/a	n/a
12	POLR2A	chr11:67164525-67167300	K562	blood:	n/a	n/a
13	POLR2A	chr11:67163695-67165813	GM12891	blood:	n/a	n/a
14	POLR2A	chr11:67163677-67167294	GM12892	blood:	n/a	n/a
15	POLR2A	chr11:67164139-67164485	H1-hESC	embryonic stem cell:	n/a	n/a
16	POLR2A	chr11:67163691-67164487	HepG2	liver:	n/a	n/a
17	POLR2A	chr11:67163943-67164796	HL-60	blood:	n/a	n/a
18	POLR2A	chr11:67164498-67165299	GM12878	blood:	n/a	n/a
19	POLR2A	chr11:67163953-67164040	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr11:67164112-67164260	A549	lung:	n/a	n/a
21	POLR2A	chr11:67162831-67167316	K562	blood:	n/a	n/a
22	POLR2A	chr11:67163806-67163900	MCF-7	breast:	n/a	n/a
23	POLR2A	chr11:67164556-67164768	HUVEC	blood vessel:	n/a	n/a
24	POLR2A	chr11:67164224-67166136	GM12891	blood:	n/a	n/a
25	POLR2A	chr11:67163972-67167371	HL-60	blood:	n/a	n/a
26	POLR2A	chr11:67164177-67164416	MCF-7	breast:	n/a	n/a
27	POLR2A	chr11:67163809-67164368	GM19193	blood:	n/a	n/a
28	POLR2A	chr11:67164608-67164680	MCF-7	breast:	n/a	n/a
29	POLR2A	chr11:67163617-67163953	A549	lung:	n/a	n/a
30	POLR2A	chr11:67163566-67164411	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr11:67162931-67167248	GM12878	blood:	n/a	n/a
32	POLR2A	chr11:67162796-67164735	ECC-1	luminal epithelium:	n/a	n/a
33	POLR2A	chr11:67163149-67167243	Hela-S3	cervix:	n/a	n/a
34	POLR2A	chr11:67163983-67164361	GM12878	blood:	n/a	n/a
35	POLR2A	chr11:67164210-67164289	GM12878	blood:	n/a	n/a
36	POLR2A	chr11:67163618-67164465	GM12878	blood:	n/a	n/a
37	POLR2A	chr11:67163544-67165831	GM12892	blood:	n/a	n/a
38	POLR2A	chr11:67164013-67164712	U87	brain:	n/a	n/a
39	POLR2A	chr11:67162599-67167265	PFSK-1	brain:	n/a	n/a
40	POLR2A	chr11:67163800-67163948	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr11:67164084-67164377	GM12892	blood:	n/a	n/a
42	POLR2A	chr11:67164563-67164724	H1-hESC	embryonic stem cell:	n/a	n/a
43	POLR2A	chr11:67164099-67164364	K562	blood:	n/a	n/a
44	POLR2A	chr11:67164183-67164504	HCT-116	colon:	n/a	n/a
45	POLR2A	chr11:67163913-67163924	MCF-7	breast:	n/a	n/a
46	POLR2A	chr11:67163568-67164468	GM12878	blood:	n/a	n/a
47	POLR2A	chr11:67164125-67164276	A549	lung:	n/a	n/a
48	POLR2A	chr11:67163768-67164711	H1-hESC	embryonic stem cell:	n/a	n/a
49	POLR2A	chr11:67163735-67164663	PANC-1	pancreas:	n/a	n/a
50	POLR2A	chr11:67164266-67164715	HUVEC	blood vessel:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr11:67032184..67035938-chr11:67163286..67166360,3	K562	blood:
2	chr11:67163742..67165862-chr11:67248927..67251919,3	K562	blood:
3	chr11:67032184..67035001-chr11:67164126..67166360,2	K562	blood:
4	chr11:67164456..67171429-chr11:67268926..67279263,19	K562	blood:
5	chr11:67164510..67166276-chr11:67272097..67273964,2	K562	blood:
6	chr11:67161941..67164521-chr11:67269135..67270716,2	K562	blood:
7	chr11:67164491..67170697-chr11:67268115..67277759,17	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-1238P	TF binding region
ENSG00000110711	chromatin interactions
ENSG00000173020	chromatin interactions
ENSG00000167797	chromatin interactions
ENSG00000110697	chromatin interactions

Extended variants
information (count: 53 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:53 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201985325	chr11:67163836-67163837	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs199635494	chr11:67163837-67163838	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs149796235	chr11:67163838-67163839	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs200617004	chr11:67163841-67163842	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs562312365	chr11:67163845-67163846	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs574429544	chr11:67163876-67163877	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs368183672	chr11:67163883-67163884	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs201858277	chr11:67163887-67163888	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs369995198	chr11:67163888-67163889	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs370979662	chr11:67163894-67163895	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs2422486	chr11:67163899-67163900	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs560079649	chr11:67163926-67163927	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs149682342	chr11:67163957-67163958	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs183696439	chr11:67163974-67163975	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs145520917	chr11:67163990-67163991	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs531653052	chr11:67164000-67164001	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs550183279	chr11:67164005-67164006	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs568469933	chr11:67164037-67164038	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs529365425	chr11:67164054-67164055	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs547908772	chr11:67164104-67164105	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs148973996	chr11:67164116-67164117	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs539595677	chr11:67164129-67164130	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs376859156	chr11:67164132-67164133	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs872109	chr11:67164133-67164134	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570000668	chr11:67164136-67164137	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs17879535	chr11:67164137-67164138	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs142939270	chr11:67164144-67164145	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs555884077	chr11:67164169-67164170	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs17881227	chr11:67164170-67164171	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs535117469	chr11:67164202-67164203	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs553786338	chr11:67164320-67164321	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs572194481	chr11:67164332-67164333	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs545985013	chr11:67164340-67164341	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs201463560	chr11:67164349-67164350	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs564305118	chr11:67164359-67164360	Enhancers Genic enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs187047678	chr11:67164405-67164406	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs543783290	chr11:67164412-67164413	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs191389624	chr11:67164414-67164415	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs17885992	chr11:67164418-67164419	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs560178110	chr11:67164455-67164456	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs529247038	chr11:67164471-67164472	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs2255990	chr11:67164495-67164496	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs78879062	chr11:67164515-67164516	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs2286617	chr11:67164523-67164524	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs533286638	chr11:67164527-67164528	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs551539007	chr11:67164552-67164553	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs75371413	chr11:67164558-67164559	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs76017242	chr11:67164591-67164592	Weak transcription Enhancers Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs367934944	chr11:67164606-67164607	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs200593199	chr11:67164615-67164616	Weak transcription Enhancers Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
small cell lung cancer	20016488	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

Chromatin state (count:167 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:67160000-67165000	Weak transcription	Aorta	Aorta
2	chr11:67160200-67165000	Weak transcription	Small Intestine	intestine
3	chr11:67160200-67166200	Weak transcription	Fetal Kidney	kidney
4	chr11:67160200-67167000	Weak transcription	Psoas Muscle	Psoas
5	chr11:67160400-67164000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr11:67160400-67164000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr11:67160400-67164000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr11:67160400-67164000	Strong transcription	Thymus	Thymus
9	chr11:67160400-67164200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr11:67160400-67164200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
11	chr11:67160400-67164200	Weak transcription	HMEC	breast
12	chr11:67160400-67164200	Weak transcription	HUVEC	blood vessel
13	chr11:67160400-67164400	Weak transcription	Duodenum Smooth Muscle	Duodenum
14	chr11:67160400-67164800	Weak transcription	Left Ventricle	heart
15	chr11:67160400-67165000	Weak transcription	Stomach Mucosa	stomach
16	chr11:67160400-67165000	Weak transcription	NHDF-Ad	bronchial
17	chr11:67160400-67165200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr11:67160400-67165200	Weak transcription	HSMMtube	muscle
19	chr11:67160400-67165200	Weak transcription	NH-A	brain
20	chr11:67160400-67165400	Weak transcription	Colon Smooth Muscle	Colon
21	chr11:67160400-67166600	Strong transcription	Brain Cingulate Gyrus	brain
22	chr11:67160400-67166800	Strong transcription	A549	lung
23	chr11:67160400-67167800	Weak transcription	Right Atrium	heart
24	chr11:67160600-67164000	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
25	chr11:67160600-67164000	Strong transcription	Fetal Intestine Small	intestine
26	chr11:67160600-67165000	Weak transcription	HSMM	muscle
27	chr11:67160600-67166800	Weak transcription	Fetal Brain Male	brain
28	chr11:67160800-67165000	Strong transcription	Skeletal Muscle Male	skeletal muscle
29	chr11:67160800-67167000	Strong transcription	Fetal Intestine Large	intestine
30	chr11:67160800-67167200	Strong transcription	HUES48 Cell Line	embryonic stem cell
31	chr11:67160800-67167200	Strong transcription	iPS-15b Cell Line	embryonic stem cell
32	chr11:67161000-67164200	Strong transcription	Primary neutrophils fromperipheralblood	blood
33	chr11:67161000-67165000	Weak transcription	Fetal Heart	heart
34	chr11:67161000-67166400	Strong transcription	Lung	lung
35	chr11:67161000-67166800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:67161000-67167400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr11:67161000-67167600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr11:67161200-67164400	Weak transcription	Primary B cells from cord blood	blood
39	chr11:67161200-67164800	Strong transcription	Cortex derived primary cultured neurospheres	brain
40	chr11:67161200-67166000	Strong transcription	Esophagus	oesophagus
41	chr11:67161200-67167000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr11:67161200-67168000	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chr11:67161400-67167000	Strong transcription	Sigmoid Colon	Sigmoid Colon
44	chr11:67161400-67167800	Strong transcription	NHEK	skin
45	chr11:67161400-67168000	Strong transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr11:67161600-67164200	Strong transcription	Primary B cells from peripheral blood	blood
47	chr11:67161600-67164800	Strong transcription	Right Ventricle	heart
48	chr11:67161600-67167800	Strong transcription	Brain Substantia Nigra	brain
49	chr11:67161800-67164000	Strong transcription	GM12878-XiMat	blood
50	chr11:67161800-67164800	Weak transcription	iPS-20b Cell Line	embryonic stem cell

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