Variant report

Variant	nsv897906
Chromosome Location	chr11:71386905-71543708
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3058)
CpG islands
(count:2078)
Chromatin interactive
region (count:10)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3058 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
2	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
3	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
4	ARID3A	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
6	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
7	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
8	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
9	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
10	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
11	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
12	ATF1	chr11:71475791-71476199	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	chr11:71511476-71511666	K562	blood:	n/a	n/a
16	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
17	ATF2	chr11:71540829-71541073	GM12878	blood:	n/a	n/a
18	ATF3	chr11:71390992-71391254	K562	blood:	n/a	n/a
19	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
20	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
21	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
24	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
25	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
26	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
27	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
28	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
29	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
30	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
31	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
32	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
33	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
34	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
35	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
36	BATF	chr11:71532357-71532883	GM12878	blood:	n/a	n/a
37	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
38	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
39	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
40	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
41	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
42	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
43	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
44	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
45	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
46	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
47	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:71426893-71427066	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:71499963-71500296	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:71497628-71497822	GM12878	blood:	n/a	n/a

(count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71462149-71462199	AG04449	skin:	fetal
2	chr11:71524971-71525021	AoSMC	blood vessel:	n/a
3	chr11:71420467-71420517	LNCaP	prostate:	n/a
4	chr11:71497552-71497602	HCM	heart:	n/a
5	chr11:71462149-71462199	AG04449	skin:	fetal
6	chr11:71524971-71525021	AoSMC	blood vessel:	n/a
7	chr11:71420467-71420517	LNCaP	prostate:	n/a
8	chr11:71497552-71497602	HCM	heart:	n/a
9	chr11:71485830-71485880	Hela-S3	cervix:	n/a
10	chr11:71462582-71462632	NB4	blood:	n/a
11	chr11:71524540-71524590	AG09309	skin:	n/a
12	chr11:71462582-71462632	ovcar-3	ovarian:	n/a
13	chr11:71522461-71522511	SKMC	muscle:	n/a
14	chr11:71421380-71421430	HMEC	breast:	n/a
15	chr11:71418204-71418254	NT2-D1	testis:	n/a
16	chr11:71524734-71524784	HCF	heart:	n/a
17	chr11:71499006-71499056	SAEC	small airway:	n/a
18	chr11:71527895-71527945	HL-60	blood:	n/a
19	chr11:71493933-71493983	T-47D	breast:	n/a
20	chr11:71524852-71524902	HRPEpiC	eye:	n/a
21	chr11:71524734-71524784	NB4	blood:	n/a
22	chr11:71543583-71543633	HCPEpiC	choroid plexus:	n/a
23	chr11:71420485-71420535	HL-60	blood:	n/a
24	chr11:71417713-71417763	HepG2	liver:	n/a
25	chr11:71511486-71511536	GM19239	blood:	n/a
26	chr11:71420467-71420517	GM06990	blood:	n/a
27	chr11:71522461-71522511	HUVEC	blood vessel:	n/a
28	chr11:71522461-71522511	RPTEC	kidney:	n/a
29	chr11:71511486-71511536	Jurkat	blood:	n/a
30	chr11:71498609-71498659	RPTEC	kidney:	n/a
31	chr11:71498715-71498765	HEK293	kidney:	embryo
32	chr11:71420947-71420997	HCT-116	colon:	n/a
33	chr11:71421380-71421430	MCF10A-Er-Src	breast:	n/a
34	chr11:71524500-71524550	HPAEpiC	pulmonary alveolar:	n/a
35	chr11:71493933-71493983	NH-A	brain:	n/a
36	chr11:71493933-71493983	SK-N-SH	brain:	n/a
37	chr11:71420485-71420535	BJ	skin:	n/a
38	chr11:71524852-71524902	CMK	blood:	n/a
39	chr11:71498202-71498252	BE2_C	brain:	n/a
40	chr11:71417713-71417763	U87	brain:	n/a
41	chr11:71524971-71525021	RPTEC	kidney:	n/a
42	chr11:71462582-71462632	ProgFib	skin:	n/a
43	chr11:71527895-71527945	SKMC	muscle:	n/a
44	chr11:71462149-71462199	HMEC	breast:	n/a
45	chr11:71417713-71417763	H1-hESC	embryonic stem cell:	embryo
46	chr11:71421380-71421430	SKMC	muscle:	n/a
47	chr11:71497552-71497602	BJ	skin:	n/a
48	chr11:71417713-71417763	AG09319	gingival:	n/a
49	chr11:71421279-71421329	CMK	blood:	n/a
50	chr11:71420467-71420517	GM19239	blood:	n/a

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

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

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
2	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
3	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
4	lnc-RP11-849H4.2.1-1	chr11:71529199-71529284	ENSG00000248671.3
5	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
6	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
7	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
8	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
9	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
10	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
11	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
12	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
13	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
14	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
15	lnc-RP11-849H4.2.1-1	chr11:71527956-71528142	ENSG00000248671.3
16	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
17	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3

No data

Variant related genes	Relation type
DEFB108B	TF binding region
FAM86C1	TF binding region
ENSG00000248671	TF binding region
ZNF705E	TF binding region
ENSG00000223235	TF binding region
ENSG00000264091	TF binding region
ENSG00000254805	TF binding region
ALG1L9P	TF binding region
ENPP7P8	TF binding region
ENSG00000254972	TF binding region
DEFB108B	CpG island
FAM86C1	CpG island
ENSG00000248671	CpG island
ZNF705E	CpG island
ENSG00000223235	CpG island
ENSG00000264091	CpG island
ENSG00000254805	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000254972	CpG island
ENSG00000158483	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000160172	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000166492	chromatin interactions

Extended variants
information (count: 7899 )
Associated
traits (count: 107 )

Variant overlapped rSNPs/rCNVs (count:7899 , 50 per page) page: 1 2 3 4 5 6 7 ... 158

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79316224	chr11:71386905-71386906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs534160920	chr11:71386933-71386934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs372348067	chr11:71386951-71386952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185813238	chr11:71386963-71386964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs7108275	chr11:71386964-71386965	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs111531341	chr11:71386983-71386984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145661950	chr11:71387002-71387003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574809270	chr11:71387004-71387005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs535921478	chr11:71387008-71387009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554348623	chr11:71387010-71387011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146753023	chr11:71387016-71387017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs200681928	chr11:71387030-71387031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs191005837	chr11:71387035-71387036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564333542	chr11:71387041-71387042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs372488863	chr11:71387088-71387089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576304147	chr11:71387101-71387102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112316212	chr11:71387111-71387112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543024776	chr11:71387150-71387151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111772325	chr11:71387174-71387175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs561705982	chr11:71387185-71387186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528919087	chr11:71387202-71387203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547077790	chr11:71387272-71387273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531235963	chr11:71387306-71387307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559066174	chr11:71387328-71387329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs534826573	chr11:71387343-71387344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527832059	chr11:71387350-71387351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199979296	chr11:71387356-71387357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183154214	chr11:71387362-71387363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs571021606	chr11:71387363-71387364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538552064	chr11:71387374-71387375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs550235121	chr11:71387398-71387399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201405300	chr11:71387411-71387412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568433281	chr11:71387432-71387433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377601421	chr11:71387464-71387465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs554262697	chr11:71387499-71387500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368767068	chr11:71387505-71387506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs201716051	chr11:71387542-71387543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572583914	chr11:71387563-71387564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539610588	chr11:71387564-71387565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs558008221	chr11:71387590-71387591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576187856	chr11:71387619-71387620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199580371	chr11:71387702-71387703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs12800368	chr11:71387720-71387721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs71473860	chr11:71387735-71387736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115719655	chr11:71387738-71387739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71473861	chr11:71387755-71387756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs71473862	chr11:71387773-71387774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs71473863	chr11:71387797-71387798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555653362	chr11:71387819-71387820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561871922	chr11:71387821-71387822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:107)

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 ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1181 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:71368200-71395600	Weak transcription	Fetal Intestine Small	intestine
2	chr11:71394000-71396800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:71395600-71396200	Enhancers	Fetal Intestine Large	intestine
4	chr11:71395600-71396200	Enhancers	Fetal Intestine Small	intestine
5	chr11:71396200-71396400	Weak transcription	Fetal Intestine Large	intestine
6	chr11:71396200-71398000	Active TSS	Fetal Intestine Small	intestine
7	chr11:71396400-71398000	Active TSS	Fetal Intestine Large	intestine
8	chr11:71396800-71404000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr11:71400200-71400600	Enhancers	K562	blood
10	chr11:71400600-71403400	Weak transcription	K562	blood
11	chr11:71403400-71403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr11:71403400-71404400	Enhancers	K562	blood
13	chr11:71404000-71404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr11:71404200-71404400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:71404200-71404600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr11:71404200-71405000	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr11:71404400-71404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr11:71404800-71409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr11:71406400-71411400	Weak transcription	Fetal Intestine Small	intestine
20	chr11:71409200-71409800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr11:71409800-71411400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:71411400-71412400	Enhancers	Fetal Intestine Small	intestine
23	chr11:71411400-71412600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr11:71411400-71412600	Enhancers	Fetal Intestine Large	intestine
25	chr11:71412400-71413200	Weak transcription	Fetal Intestine Small	intestine
26	chr11:71413200-71415800	ZNF genes & repeats	Fetal Intestine Small	intestine
27	chr11:71414800-71416000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr11:71415400-71415600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr11:71415400-71416000	Enhancers	K562	blood
30	chr11:71415400-71416400	Enhancers	Fetal Intestine Large	intestine
31	chr11:71415600-71416200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr11:71415800-71416000	Weak transcription	Fetal Intestine Small	intestine
33	chr11:71416000-71416400	Flanking Active TSS	K562	blood
34	chr11:71416000-71416600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr11:71416000-71417000	Enhancers	Fetal Intestine Small	intestine
36	chr11:71416200-71416400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr11:71416400-71417400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr11:71416400-71417400	Weak transcription	Fetal Intestine Large	intestine
39	chr11:71416400-71417400	Enhancers	K562	blood
40	chr11:71416600-71417400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr11:71417000-71417400	Weak transcription	Fetal Intestine Small	intestine
42	chr11:71417000-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr11:71417200-71417600	Enhancers	Fetal Lung	lung
44	chr11:71417200-71417800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr11:71417200-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr11:71417400-71417600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr11:71417400-71417800	Flanking Active TSS	K562	blood
48	chr11:71417400-71418000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr11:71417400-71418000	Genic enhancers	Fetal Intestine Small	intestine
50	chr11:71417400-71421000	Enhancers	Fetal Intestine Large	intestine

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