Variant report

Variant	nsv1044072
Chromosome Location	chr11:71379653-71527699
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3003)
CpG islands
(count:1895)
Chromatin interactive
region (count:10)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3003 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

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	chr11:71499570-71499575	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:71460269-71460401	K562	blood:	n/a	n/a
4	ARID3A	chr11:71454526-71454806	K562	blood:	n/a	n/a
5	ARID3A	chr11:71423449-71423649	K562	blood:	n/a	n/a
6	ARID3A	chr11:71416385-71416810	K562	blood:	n/a	n/a
7	ARID3A	chr11:71511545-71511692	K562	blood:	n/a	n/a
8	ARID3A	chr11:71410234-71410262	K562	blood:	n/a	n/a
9	ARID3A	chr11:71417122-71417426	K562	blood:	n/a	n/a
10	ARID3A	chr11:71475957-71476045	K562	blood:	n/a	n/a
11	ATF1	chr11:71511476-71511666	K562	blood:	n/a	n/a
12	ATF1	chr11:71475791-71476199	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	chr11:71430611-71430715	K562	blood:	n/a	n/a
16	ATF1	chr11:71417251-71417305	K562	blood:	n/a	n/a
17	ATF3	chr11:71390992-71391254	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	ATF3	chr11:71416472-71416725	K562	blood:	n/a	n/a
21	BACH1	chr11:71421452-71421711	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr11:71428825-71429020	GM12878	blood:	n/a	chr11:71428919-71428927
23	BATF	chr11:71499485-71499773	GM12878	blood:	n/a	n/a
24	BATF	chr11:71498902-71499183	GM12878	blood:	n/a	n/a
25	BATF	chr11:71524810-71525112	GM12878	blood:	n/a	n/a
26	BATF	chr11:71445516-71445843	GM12878	blood:	n/a	n/a
27	BATF	chr11:71503748-71504008	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	chr11:71426836-71427105	GM12878	blood:	n/a	n/a
31	BATF	chr11:71511440-71511763	GM12878	blood:	n/a	n/a
32	BATF	chr11:71407057-71407555	GM12878	blood:	n/a	n/a
33	BATF	chr11:71398772-71399069	GM12878	blood:	n/a	n/a
34	BATF	chr11:71496443-71496643	GM12878	blood:	n/a	n/a
35	BATF	chr11:71457474-71457675	GM12878	blood:	n/a	n/a
36	BATF	chr11:71425014-71425933	GM12878	blood:	n/a	n/a
37	BATF	chr11:71426864-71427152	GM12878	blood:	n/a	n/a
38	BATF	chr11:71421930-71422331	GM12878	blood:	n/a	n/a
39	BATF	chr11:71421908-71422351	GM12878	blood:	n/a	n/a
40	BATF	chr11:71428726-71429101	GM12878	blood:	n/a	chr11:71428919-71428927
41	BATF	chr11:71445512-71445867	GM12878	blood:	n/a	n/a
42	BATF	chr11:71421266-71421667	GM12878	blood:	n/a	n/a
43	BATF	chr11:71425385-71425877	GM12878	blood:	n/a	n/a
44	BATF	chr11:71456494-71456680	GM12878	blood:	n/a	n/a
45	BCL11A	chr11:71445521-71445844	GM12878	blood:	n/a	n/a
46	BCL11A	chr11:71497628-71497822	GM12878	blood:	n/a	n/a
47	BCL11A	chr11:71511419-71511802	GM12878	blood:	n/a	n/a
48	BCL11A	chr11:71422007-71422279	GM12878	blood:	n/a	n/a
49	BCL11A	chr11:71426893-71427066	GM12878	blood:	n/a	n/a
50	BCL11A	chr11:71498971-71499169	GM12878	blood:	n/a	n/a

(count:1895 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:71421279-71421329	BJ	skin:	n/a
2	chr11:71418204-71418254	Hela-S3	cervix:	n/a
3	chr11:71497575-71497625	HPAEpiC	pulmonary alveolar:	n/a
4	chr11:71502816-71502866	GM12878	blood:	n/a
5	chr11:71421279-71421329	BJ	skin:	n/a
6	chr11:71418204-71418254	Hela-S3	cervix:	n/a
7	chr11:71497575-71497625	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:71502816-71502866	GM12878	blood:	n/a
9	chr11:71418204-71418254	AG09319	gingival:	n/a
10	chr11:71498202-71498252	HRCEpiC	kidney:	n/a
11	chr11:71498715-71498765	HRE	kidney:	n/a
12	chr11:71524852-71524902	RPTEC	kidney:	n/a
13	chr11:71498715-71498765	HCM	heart:	n/a
14	chr11:71524852-71524902	HCT-116	colon:	n/a
15	chr11:71499117-71499167	MCF-7	breast:	n/a
16	chr11:71421279-71421329	HRPEpiC	eye:	n/a
17	chr11:71524852-71524902	Hela-S3	cervix:	n/a
18	chr11:71498609-71498659	Caco-2	colon:	n/a
19	chr11:71420467-71420517	MCF-7	breast:	n/a
20	chr11:71499006-71499056	HUVEC	blood vessel:	n/a
21	chr11:71462582-71462632	HRCEpiC	kidney:	n/a
22	chr11:71497575-71497625	U87	brain:	n/a
23	chr11:71417713-71417763	U87	brain:	n/a
24	chr11:71462149-71462199	HRCEpiC	kidney:	n/a
25	chr11:71524734-71524784	GM12878	blood:	n/a
26	chr11:71420947-71420997	AG09309	skin:	n/a
27	chr11:71417657-71417707	AG04450	lung:	fetal
28	chr11:71462582-71462632	PANC-1	pancreas:	n/a
29	chr11:71524971-71525021	NH-A	brain:	n/a
30	chr11:71421380-71421430	HCT-116	colon:	n/a
31	chr11:71417657-71417707	SK-N-SH	brain:	n/a
32	chr11:71418204-71418254	Hepatocyte	liver:	n/a
33	chr11:71417713-71417763	HRE	kidney:	n/a
34	chr11:71485830-71485880	AoSMC	blood vessel:	n/a
35	chr11:71502816-71502866	ProgFib	skin:	n/a
36	chr11:71524734-71524784	PFSK-1	brain:	n/a
37	chr11:71493933-71493983	PFSK-1	brain:	n/a
38	chr11:71497688-71497738	HMEC	breast:	n/a
39	chr11:71456947-71456997	NB4	blood:	n/a
40	chr11:71462549-71462599	BJ	skin:	n/a
41	chr11:71524500-71524550	NT2-D1	testis:	n/a
42	chr11:71421380-71421430	MCF10A-Er-Src	breast:	n/a
43	chr11:71456947-71456997	GM12891	blood:	n/a
44	chr11:71502816-71502866	PrEC	prostate:	n/a
45	chr11:71457160-71457210	HepG2	liver:	n/a
46	chr11:71456947-71456997	SK-N-SH	brain:	n/a
47	chr11:71417657-71417707	GM12878	blood:	n/a
48	chr11:71417713-71417763	HRPEpiC	eye:	n/a
49	chr11:71522461-71522511	Caco-2	colon:	n/a
50	chr11:71497575-71497625	Hela-S3	cervix:	n/a

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

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

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM86C1-4	chr11:71393417-71393825	expRegAs_chr11_7370_+
2	lnc-AP000867.1-1	chr11:71415223-71415306	ENSG00000254972
3	lnc-RP11-849H4.2.1-1	chr11:71517696-71518702	NONHSAT022713
4	lnc-FAM86C1-1	chr11:71425421-71425604	NONHSAT022701
5	lnc-AP000867.1-1	chr11:71416406-71416450	ENSG00000254972
6	lnc-AP000867.1-2	chr11:71383721-71384047	ENSG00000254504.1
7	lnc-FAM86C1-5	chr11:71392883-71393202	expRegAs_chr11_7367_+
8	lnc-RP11-849H4.2.1-1	chr11:71524389-71524529	NONHSAT022713
9	lnc-AP000867.1-1	chr11:71412314-71412531	ENSG00000254972
10	lnc-AP000867.1-2	chr11:71421533-71421627	ENSG00000254504.1
11	lnc-FAM86C1-1	chr11:71422786-71422863	NONHSAT022701
12	lnc-FAM86C1-3	chr11:71394183-71394998	expRegAs_chr11_7373_+
13	lnc-FAM86C1-2	chr11:71395710-71396117	expRegAs_chr11_7374_+
14	lnc-AP000867.1-4	chr11:71401499-71401703	NONHSAT022697
15	lnc-FAM86C1-1	chr11:71433219-71433273	NONHSAT022701
16	lnc-RP11-849H4.2.1-1	chr11:71518637-71518702	ENSG00000248671.3

No data

Variant related genes	Relation type
FAM86C1	TF binding region
ENSG00000248671	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
RPS3AP41	TF binding region
FAM86C1	CpG island
ENSG00000248671	CpG island
ENSG00000223235	CpG island
ENSG00000264091	CpG island
ENSG00000254805	CpG island
ALG1L9P	CpG island
ENPP7P8	CpG island
ENSG00000254972	CpG island
RPS3AP41	CpG island
ENSG00000158483	chromatin interactions
ENSG00000244026	chromatin interactions
ENSG00000248671	chromatin interactions
ENSG00000130522	chromatin interactions
ENSG00000118894	chromatin interactions
ENSG00000160172	chromatin interactions
ENSG00000166492	chromatin interactions

Extended variants
information (count: 7953 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:7953 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4121485	chr11:71379653-71379654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570402301	chr11:71379664-71379665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113040552	chr11:71379710-71379711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs549398230	chr11:71379713-71379714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1940181	chr11:71379715-71379716	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs535132964	chr11:71379736-71379737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10792818	chr11:71379752-71379753	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs577755268	chr11:71379754-71379755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs138110714	chr11:71379804-71379805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs113016424	chr11:71379808-71379809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs59084692	chr11:71379811-71379812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534674953	chr11:71379826-71379827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556837624	chr11:71379893-71379894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182741637	chr11:71379904-71379905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542175790	chr11:71379912-71379913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149184971	chr11:71379920-71379921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs115519671	chr11:71379946-71379947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs540299778	chr11:71379956-71379957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs187813059	chr11:71379957-71379958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2155421	chr11:71379962-71379963	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs552050238	chr11:71380027-71380028	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs10898423	chr11:71380041-71380042	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs531238945	chr11:71380064-71380065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs563604006	chr11:71380075-71380076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567671385	chr11:71380088-71380089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4620743	chr11:71380106-71380107	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547064277	chr11:71380107-71380108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs143069396	chr11:71380122-71380123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs538400175	chr11:71380129-71380130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58110994	chr11:71380170-71380171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs202212662	chr11:71380189-71380190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs57688149	chr11:71380199-71380200	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs568778185	chr11:71380218-71380219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182577277	chr11:71380224-71380225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200403735	chr11:71380235-71380236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs187577908	chr11:71380263-71380264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572780439	chr11:71380276-71380277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35916038	chr11:71380278-71380279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539888742	chr11:71380286-71380287	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35056526	chr11:71380287-71380288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191994241	chr11:71380293-71380294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111818432	chr11:71380304-71380305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs34671669	chr11:71380316-71380317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113206864	chr11:71380319-71380320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs148080274	chr11:71380322-71380323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs36117918	chr11:71380334-71380335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184929411	chr11:71380336-71380337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528484601	chr11:71380379-71380380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200528797	chr11:71380393-71380394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs190546464	chr11:71380399-71380400	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:1168 , 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	chr11:71385800-71386000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
3	chr11:71394000-71396800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr11:71395600-71396200	Enhancers	Fetal Intestine Large	intestine
5	chr11:71395600-71396200	Enhancers	Fetal Intestine Small	intestine
6	chr11:71396200-71396400	Weak transcription	Fetal Intestine Large	intestine
7	chr11:71396200-71398000	Active TSS	Fetal Intestine Small	intestine
8	chr11:71396400-71398000	Active TSS	Fetal Intestine Large	intestine
9	chr11:71396800-71404000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:71400200-71400600	Enhancers	K562	blood
11	chr11:71400600-71403400	Weak transcription	K562	blood
12	chr11:71403400-71403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr11:71403400-71404400	Enhancers	K562	blood
14	chr11:71404000-71404800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:71404200-71404400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr11:71404200-71404600	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:71404200-71405000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr11:71404400-71404800	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr11:71404800-71409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr11:71406400-71411400	Weak transcription	Fetal Intestine Small	intestine
21	chr11:71409200-71409800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr11:71409800-71411400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr11:71411400-71412400	Enhancers	Fetal Intestine Small	intestine
24	chr11:71411400-71412600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr11:71411400-71412600	Enhancers	Fetal Intestine Large	intestine
26	chr11:71412400-71413200	Weak transcription	Fetal Intestine Small	intestine
27	chr11:71413200-71415800	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr11:71414800-71416000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr11:71415400-71415600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr11:71415400-71416000	Enhancers	K562	blood
31	chr11:71415400-71416400	Enhancers	Fetal Intestine Large	intestine
32	chr11:71415600-71416200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr11:71415800-71416000	Weak transcription	Fetal Intestine Small	intestine
34	chr11:71416000-71416400	Flanking Active TSS	K562	blood
35	chr11:71416000-71416600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr11:71416000-71417000	Enhancers	Fetal Intestine Small	intestine
37	chr11:71416200-71416400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr11:71416400-71417400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr11:71416400-71417400	Weak transcription	Fetal Intestine Large	intestine
40	chr11:71416400-71417400	Enhancers	K562	blood
41	chr11:71416600-71417400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:71417000-71417400	Weak transcription	Fetal Intestine Small	intestine
43	chr11:71417000-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr11:71417200-71417600	Enhancers	Fetal Lung	lung
45	chr11:71417200-71417800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr11:71417200-71418400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr11:71417400-71417600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr11:71417400-71417800	Flanking Active TSS	K562	blood
49	chr11:71417400-71418000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr11:71417400-71418000	Genic enhancers	Fetal Intestine Small	intestine

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