Variant report

Variant	nsv1047177
Chromosome Location	chr11:71360190-71513585
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2736)
CpG islands
(count:1530)
Chromatin interactive
region (count:10)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2736 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
2	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
3	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
4	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
5	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
6	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
7	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
8	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
9	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
10	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
11	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
12	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
13	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
14	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
15	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
16	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
17	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
18	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
20	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
21	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
23	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
24	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
25	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
26	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
27	BATF	chr11:71364307-71364538	GM12878	blood:	n/a	n/a
28	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
29	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
30	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
31	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
32	BATF	chr11:71376106-71376750	GM12878	blood:	n/a	n/a
33	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
34	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
35	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
36	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
37	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
38	BATF	chr11:71364018-71364247	GM12878	blood:	n/a	chr11:71364110-71364121
39	BATF	chr11:71376144-71376697	GM12878	blood:	n/a	n/a
40	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
41	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
42	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
43	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
44	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
45	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
46	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
47	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:71511333-71511561	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:71511419-71511802	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:71376209-71376453	GM12878	blood:	n/a	n/a

(count:1530 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71420947-71420997	MCF10A-Er-Src	breast:	n/a
2	chr11:71456947-71456997	NHDF-neo	bronchial:	n/a
3	chr11:71499117-71499167	Jurkat	blood:	n/a
4	chr11:71485830-71485880	HUVEC	blood vessel:	n/a
5	chr11:71417657-71417707	ECC-1	luminal epithelium:	n/a
6	chr11:71420947-71420997	MCF10A-Er-Src	breast:	n/a
7	chr11:71456947-71456997	NHDF-neo	bronchial:	n/a
8	chr11:71499117-71499167	Jurkat	blood:	n/a
9	chr11:71485830-71485880	HUVEC	blood vessel:	n/a
10	chr11:71417657-71417707	ECC-1	luminal epithelium:	n/a
11	chr11:71417657-71417707	GM19239	blood:	n/a
12	chr11:71456947-71456997	Jurkat	blood:	n/a
13	chr11:71457160-71457210	PANC-1	pancreas:	n/a
14	chr11:71498202-71498252	HEEpiC	esophagus:	n/a
15	chr11:71485830-71485880	ECC-1	luminal epithelium:	n/a
16	chr11:71498715-71498765	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:71418204-71418254	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:71418204-71418254	MCF10A-Er-Src	breast:	n/a
19	chr11:71499117-71499167	H1-hESC	embryonic stem cell:	embryo
20	chr11:71511486-71511536	HCF	heart:	n/a
21	chr11:71497552-71497602	AG04449	skin:	fetal
22	chr11:71462149-71462199	AG04449	skin:	fetal
23	chr11:71420467-71420517	HMEC	breast:	n/a
24	chr11:71417713-71417763	ovcar-3	ovarian:	n/a
25	chr11:71499117-71499167	BE2_C	brain:	n/a
26	chr11:71485830-71485880	HIPEpiC	eye:	n/a
27	chr11:71462582-71462632	HRPEpiC	eye:	n/a
28	chr11:71420947-71420997	SK-N-SH	brain:	n/a
29	chr11:71462582-71462632	NT2-D1	testis:	n/a
30	chr11:71420467-71420517	SK-N-MC	brain:	n/a
31	chr11:71417713-71417763	HIPEpiC	eye:	n/a
32	chr11:71418204-71418254	ECC-1	luminal epithelium:	n/a
33	chr11:71457160-71457210	T-47D	breast:	n/a
34	chr11:71462149-71462199	HCT-116	colon:	n/a
35	chr11:71420485-71420535	NHBE	bronchial:	n/a
36	chr11:71456947-71456997	HEK293	kidney:	embryo
37	chr11:71498715-71498765	GM12878	blood:	n/a
38	chr11:71498715-71498765	SK-N-MC	brain:	n/a
39	chr11:71497688-71497738	GM06990	blood:	n/a
40	chr11:71420467-71420517	HL-60	blood:	n/a
41	chr11:71498715-71498765	NH-A	brain:	n/a
42	chr11:71499117-71499167	AoSMC	blood vessel:	n/a
43	chr11:71498202-71498252	HCF	heart:	n/a
44	chr11:71420947-71420997	NHBE	bronchial:	n/a
45	chr11:71456947-71456997	HCPEpiC	choroid plexus:	n/a
46	chr11:71498715-71498765	U87	brain:	n/a
47	chr11:71420467-71420517	HUVEC	blood vessel:	n/a
48	chr11:71462549-71462599	Jurkat	blood:	n/a
49	chr11:71493933-71493983	GM06990	blood:	n/a
50	chr11:71420947-71420997	PANC-1	pancreas:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:3442224..3443750-chr11:71497854..71499382,2	MCF-7	breast:
2	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
3	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
4	chr11:71502585..71504558-chr11:71523085..71525009,2	MCF-7	breast:
5	chr11:71499803..71501328-chr11:71502237..71504426,2	K562	blood:
6	chr11:71498143..71498944-chr16:5147397..5148064,2	Hela-S3	cervix:
7	chr11:71349980..71350709-chr11:71511135..71512071,2	K562	blood:
8	chr11:67572484..67573077-chr11:71498421..71498985,2	HCT-116	colon:
9	chr11:71498340..71499087-chr19:18391666..18392636,2	Hela-S3	cervix:
10	chr11:71489714..71493464-chr11:71497648..71499552,3	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
2	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
3	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
4	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
5	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
6	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
7	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
8	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
9	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
10	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
11	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
12	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
13	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+

No data

Variant related genes	Relation type
ENSG00000254805	TF binding region
ENPP7P8	TF binding region
ENSG00000221458	TF binding region
FAM86C1	TF binding region
ENSG00000223235	TF binding region
ENSG00000254972	TF binding region
RPS3AP41	TF binding region
ENSG00000254805	CpG island
ENPP7P8	CpG island
ENSG00000221458	CpG island
FAM86C1	CpG island
ENSG00000223235	CpG island
ENSG00000254972	CpG island
RPS3AP41	CpG island
ENSG00000244026	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000166492	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000160172	chromatin interactions

Extended variants
information (count: 8304 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:8304 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7105749	chr11:71360190-71360191	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs571124061	chr11:71360203-71360204	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs141736371	chr11:71360226-71360227	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556569072	chr11:71360248-71360249	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147095993	chr11:71360253-71360254	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535983290	chr11:71360259-71360260	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2000591	chr11:71360269-71360270	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs573900109	chr11:71360281-71360282	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181473824	chr11:71360310-71360311	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs370311069	chr11:71360313-71360314	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs375516310	chr11:71360319-71360320	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs186952672	chr11:71360333-71360334	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs7928659	chr11:71360350-71360351	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs563711001	chr11:71360351-71360352	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571258201	chr11:71360355-71360356	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs143294902	chr11:71360367-71360368	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148286925	chr11:71360446-71360447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192096032	chr11:71360481-71360482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs528306442	chr11:71360487-71360488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183995262	chr11:71360530-71360531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572148102	chr11:71360535-71360536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs540594593	chr11:71360551-71360552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141423320	chr11:71360599-71360600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs150584726	chr11:71360610-71360611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550151741	chr11:71360611-71360612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568522741	chr11:71360626-71360627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113506506	chr11:71360645-71360646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529256092	chr11:71360652-71360653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535897660	chr11:71360656-71360657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60845299	chr11:71360666-71360667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs35745148	chr11:71360667-71360668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs12574357	chr11:71360677-71360678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141885280	chr11:71360681-71360682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111331031	chr11:71360686-71360687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs58675335	chr11:71360687-71360688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs34852364	chr11:71360706-71360707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554267798	chr11:71360707-71360708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34200851	chr11:71360711-71360712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76576985	chr11:71360716-71360717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535197018	chr11:71360719-71360720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs368376218	chr11:71360768-71360769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548001344	chr11:71360797-71360798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs578189250	chr11:71360811-71360812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554783442	chr11:71360841-71360842	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs576166169	chr11:71360854-71360855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs141741232	chr11:71360859-71360860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185399890	chr11:71360861-71360862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs561354440	chr11:71360883-71360884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528607716	chr11:71360884-71360885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs75456460	chr11:71360904-71360905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Smith-Lemli-Opitz syndrome	21572526	CNVD
Glioblastoma multiforme	21080181	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chordoma	21602918	CNVD
Metanephric adenoma	20802469	CNVD
Melanoma	18172304	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
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	16620391	CNVD
Multiple myeloma	17550852	CNVD
Neuroblastoma	18923191	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Multiple myeloma	16616336	CNVD
Urothelial cell carcinoma	18451213	CNVD
Leukoplakia	24403051	CNVD
Prostate cancer	17217626	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:985 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71354000-71366400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr11:71359000-71360400	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr11:71359200-71360200	Enhancers	Stomach Mucosa	stomach
4	chr11:71359600-71360400	Enhancers	Rectal Mucosa Donor 29	rectum
5	chr11:71359800-71360400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr11:71359800-71367600	Weak transcription	Fetal Intestine Small	intestine
7	chr11:71360000-71360200	Enhancers	Lung	lung
8	chr11:71360400-71362000	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr11:71360400-71373000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:71362200-71362400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr11:71362400-71362800	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr11:71363600-71364600	Enhancers	GM12878-XiMat	blood
13	chr11:71366400-71366800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr11:71366400-71367800	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr11:71367200-71367400	Enhancers	Fetal Intestine Large	intestine
16	chr11:71367200-71367800	Enhancers	A549	lung
17	chr11:71367400-71367600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr11:71367600-71368000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr11:71367600-71368200	Enhancers	Fetal Intestine Small	intestine
20	chr11:71368000-71368200	Enhancers	Fetal Intestine Large	intestine
21	chr11:71368200-71395600	Weak transcription	Fetal Intestine Small	intestine
22	chr11:71385800-71386000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
23	chr11:71394000-71396800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:71395600-71396200	Enhancers	Fetal Intestine Large	intestine
25	chr11:71395600-71396200	Enhancers	Fetal Intestine Small	intestine
26	chr11:71396200-71396400	Weak transcription	Fetal Intestine Large	intestine
27	chr11:71396200-71398000	Active TSS	Fetal Intestine Small	intestine
28	chr11:71396400-71398000	Active TSS	Fetal Intestine Large	intestine
29	chr11:71396800-71404000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr11:71400200-71400600	Enhancers	K562	blood
31	chr11:71400600-71403400	Weak transcription	K562	blood
32	chr11:71403400-71403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr11:71403400-71404400	Enhancers	K562	blood
34	chr11:71404000-71404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:71404200-71404400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr11:71404200-71404600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr11:71404200-71405000	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr11:71404400-71404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr11:71404800-71409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr11:71406400-71411400	Weak transcription	Fetal Intestine Small	intestine
41	chr11:71409200-71409800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:71409800-71411400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr11:71411400-71412400	Enhancers	Fetal Intestine Small	intestine
44	chr11:71411400-71412600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr11:71411400-71412600	Enhancers	Fetal Intestine Large	intestine
46	chr11:71412400-71413200	Weak transcription	Fetal Intestine Small	intestine
47	chr11:71413200-71415800	ZNF genes & repeats	Fetal Intestine Small	intestine
48	chr11:71414800-71416000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr11:71415400-71415600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr11:71415400-71416000	Enhancers	K562	blood

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