Variant report

Variant	nsv1045511
Chromosome Location	chr11:71395657-71527896
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2983)
CpG islands
(count:1953)
Chromatin interactive
region (count:10)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2983 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:71423994-71424313	K562	blood:	n/a	n/a
2	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
3	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
4	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
5	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
6	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
7	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
8	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
9	ARID3A	chr11:71499570-71499575	HepG2	liver:	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	chr11:71511476-71511666	K562	blood:	n/a	n/a
13	ATF1	chr11:71483232-71483430	K562	blood:	n/a	n/a
14	ATF1	chr11:71454569-71454834	K562	blood:	n/a	n/a
15	ATF1	chr11:71475791-71476199	K562	blood:	n/a	n/a
16	ATF1	chr11:71430611-71430715	K562	blood:	n/a	n/a
17	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
18	ATF3	chr11:71511455-71511719	H1-hESC	embryonic stem cell:	n/a	n/a
19	ATF3	chr11:71511454-71511674	GM12878	blood:	n/a	n/a
20	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
21	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
22	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
23	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
24	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
25	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
26	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
27	BATF	chr11:71527794-71528002	GM12878	blood:	n/a	chr11:71527879-71527890
28	BATF	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
29	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
30	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
31	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
32	BATF	chr11:71398779-71399009	GM12878	blood:	n/a	n/a
33	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
34	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
35	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
36	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
37	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
38	BATF	chr11:71503748-71504008	GM12878	blood:	n/a	n/a
39	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
40	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
41	BATF	chr11:71499406-71499609	GM12878	blood:	n/a	n/a
42	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
43	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
44	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:71511333-71511561	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:71421911-71422277	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:71428570-71428787	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:71428574-71429024	GM12878	blood:	n/a	chr11:71428833-71428842
49	BCL11A	chr11:71498971-71499169	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:71406992-71407565	GM12878	blood:	n/a	n/a

(count:1953 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71457160-71457210	HepG2	liver:	n/a
2	chr11:71457160-71457210	HepG2	liver:	n/a
3	chr11:71420947-71420997	BE2_C	brain:	n/a
4	chr11:71421380-71421430	HEK293	kidney:	embryo
5	chr11:71420485-71420535	GM12878	blood:	n/a
6	chr11:71522461-71522511	NHBE	bronchial:	n/a
7	chr11:71462549-71462599	HCT-116	colon:	n/a
8	chr11:71497688-71497738	HPAEpiC	pulmonary alveolar:	n/a
9	chr11:71457160-71457210	SK-N-SH	brain:	n/a
10	chr11:71511486-71511536	AoSMC	blood vessel:	n/a
11	chr11:71420947-71420997	AG09309	skin:	n/a
12	chr11:71421380-71421430	ProgFib	skin:	n/a
13	chr11:71524734-71524784	AG10803	skin:	n/a
14	chr11:71421279-71421329	CMK	blood:	n/a
15	chr11:71524852-71524902	SKMC	muscle:	n/a
16	chr11:71522461-71522511	ProgFib	skin:	n/a
17	chr11:71498609-71498659	SAEC	small airway:	n/a
18	chr11:71497552-71497602	SK-N-MC	brain:	n/a
19	chr11:71462582-71462632	T-47D	breast:	n/a
20	chr11:71522461-71522511	Hela-S3	cervix:	n/a
21	chr11:71497688-71497738	T-47D	breast:	n/a
22	chr11:71499117-71499167	K562	blood:	n/a
23	chr11:71420947-71420997	SKMC	muscle:	n/a
24	chr11:71497688-71497738	GM19239	blood:	n/a
25	chr11:71497688-71497738	HUVEC	blood vessel:	n/a
26	chr11:71511486-71511536	HMEC	breast:	n/a
27	chr11:71497552-71497602	SK-N-SH	brain:	n/a
28	chr11:71418204-71418254	AG04450	lung:	fetal
29	chr11:71522461-71522511	HCPEpiC	choroid plexus:	n/a
30	chr11:71420947-71420997	HRE	kidney:	n/a
31	chr11:71462549-71462599	HRE	kidney:	n/a
32	chr11:71417657-71417707	AG04449	skin:	fetal
33	chr11:71499117-71499167	Hepatocyte	liver:	n/a
34	chr11:71527895-71527945	AG09319	gingival:	n/a
35	chr11:71497688-71497738	SK-N-SH_RA	brain:	n/a
36	chr11:71462549-71462599	AG04449	skin:	fetal
37	chr11:71421380-71421430	HCM	heart:	n/a
38	chr11:71457160-71457210	SK-N-SH_RA	brain:	n/a
39	chr11:71522461-71522511	HCT-116	colon:	n/a
40	chr11:71462549-71462599	HCF	heart:	n/a
41	chr11:71493933-71493983	HCPEpiC	choroid plexus:	n/a
42	chr11:71524540-71524590	AoSMC	blood vessel:	n/a
43	chr11:71524500-71524550	IMR90	lung:	fetal
44	chr11:71462549-71462599	NHDF-neo	bronchial:	n/a
45	chr11:71421279-71421329	AG04450	lung:	fetal
46	chr11:71497688-71497738	PrEC	prostate:	n/a
47	chr11:71420947-71420997	NHDF-neo	bronchial:	n/a
48	chr11:71522461-71522511	SAEC	small airway:	n/a
49	chr11:71497552-71497602	HCPEpiC	choroid plexus:	n/a
50	chr11:71524852-71524902	BJ	skin:	n/a

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

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

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3
2	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
3	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
4	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
5	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
6	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
7	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
8	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
9	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
10	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
11	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
12	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1

No data

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

Extended variants
information (count: 7084 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7084 , 50 per page) page: 1 2 3 4 5 6 7 ... 142

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565018836	chr11:71395669-71395670	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565072840	chr11:71395703-71395704	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577003568	chr11:71395735-71395736	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs371845437	chr11:71395753-71395754	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs59414029	chr11:71395762-71395763	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs544513644	chr11:71395787-71395788	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs562776479	chr11:71395794-71395795	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs11501835	chr11:71395799-71395800	ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs564558454	chr11:71395817-71395818	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs548225980	chr11:71395910-71395911	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs191430425	chr11:71395920-71395921	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs11501719	chr11:71395993-71395994	ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs11501836	chr11:71396003-71396004	ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs571803525	chr11:71396029-71396030	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs184070070	chr11:71396042-71396043	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs11501720	chr11:71396045-71396046	ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188963590	chr11:71396052-71396053	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs192456895	chr11:71396079-71396080	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs55659919	chr11:71396098-71396099	ZNF genes & repeats Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs182316919	chr11:71396107-71396108	ZNF genes & repeats Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
21	rs373724283	chr11:71396134-71396135	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs200314542	chr11:71396135-71396136	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374921600	chr11:71396136-71396137	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534287397	chr11:71396186-71396187	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185301200	chr11:71396213-71396214	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs558829551	chr11:71396226-71396227	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs55892748	chr11:71396257-71396258	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs544430121	chr11:71396272-71396273	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs191149567	chr11:71396301-71396302	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs562740733	chr11:71396323-71396324	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs138494400	chr11:71396324-71396325	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs142956030	chr11:71396367-71396368	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs560078123	chr11:71396392-71396393	ZNF genes & repeats Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs527337874	chr11:71396410-71396411	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs545881689	chr11:71396411-71396412	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs564034267	chr11:71396417-71396418	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs532703400	chr11:71396419-71396420	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs550783819	chr11:71396427-71396428	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs183321208	chr11:71396433-71396434	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs113308058	chr11:71396457-71396458	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs376437852	chr11:71396475-71396476	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs186161605	chr11:71396513-71396514	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs530311972	chr11:71396561-71396562	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs376574144	chr11:71396565-71396566	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs548508099	chr11:71396594-71396595	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs12806271	chr11:71396606-71396607	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs12800600	chr11:71396612-71396613	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs566853840	chr11:71396647-71396648	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs533941482	chr11:71396651-71396652	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs111707490	chr11:71396662-71396663	ZNF genes & repeats Active TSS	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 ductal adenocarcinoma	19077451	CNVD
Breast cancer	17142309	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	21781307	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1166 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

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

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