Variant report

Variant	nsv949437
Chromosome Location	chr11:55780469-56042980
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr11:55856682-55856750	K562	blood:	n/a	n/a
2	BACH1	chr11:55937213-55937236	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr11:55919802-55920154	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr11:56000780-56000794	K562	blood:	n/a	n/a
5	BACH1	chr11:55917916-55917973	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:55997409-55997769	K562	blood:	n/a	chr11:55997577-55997588
7	CEBPB	chr11:55964899-55965188	A549	lung:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
8	CEBPB	chr11:55964893-55965195	H1-hESC	embryonic stem cell:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
9	CEBPB	chr11:55906014-55906261	A549	lung:	n/a	n/a
10	CEBPB	chr11:55997392-55997743	A549	lung:	n/a	chr11:55997577-55997588
11	CEBPB	chr11:55997392-55997747	IMR90	lung:	n/a	chr11:55997577-55997588
12	CEBPB	chr11:55997403-55997756	HepG2	liver:	n/a	chr11:55997577-55997588
13	CEBPB	chr11:55921214-55921534	HepG2	liver:	n/a	chr11:55921389-55921400
14	CEBPB	chr11:55997407-55997695	Hela-S3	cervix:	n/a	chr11:55997577-55997588
15	CEBPB	chr11:55823995-55824138	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr11:55964901-55965149	Hela-S3	cervix:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
17	CEBPB	chr11:55964876-55965231	IMR90	lung:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
18	CEBPB	chr11:55828199-55828299	K562	blood:	n/a	n/a
19	CEBPB	chr11:55834333-55834597	HepG2	liver:	n/a	n/a
20	CEBPB	chr11:55997458-55997740	H1-hESC	embryonic stem cell:	n/a	chr11:55997577-55997588
21	CEBPB	chr11:55905952-55906317	MCF-7	breast:	n/a	n/a
22	CEBPB	chr11:55807323-55807629	HepG2	liver:	n/a	chr11:55807438-55807449
23	CEBPB	chr11:55964882-55965215	HepG2	liver:	n/a	chr11:55965053-55965066 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965055-55965064 chr11:55965054-55965065
24	CHD1	chr11:55861285-55861372	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr11:55824010-55824142	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr11:55807160-55807183	GM10248	blood:	n/a	n/a
27	CTCF	chr11:55857282-55857482	IMR90	lung:	n/a	chr11:55857306-55857313
28	CTCF	chr11:55939440-55939590	GM12865	blood:	n/a	n/a
29	CTCF	chr11:55857300-55857450	GM12801	blood:	n/a	chr11:55857306-55857313
30	CTCF	chr11:55835352-55835424	ProgFib	skin:	n/a	n/a
31	CTCF	chr11:55893760-55893910	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr11:55857328-55857425	GM20000	blood:	n/a	n/a
33	CTCF	chr11:56032960-56033110	Caco-2	colon:	n/a	n/a
34	CTCF	chr11:55857304-55857452	LNCaP	prostate:	n/a	chr11:55857306-55857313
35	CTCF	chr11:55923930-55924003	GM13977	blood:	n/a	n/a
36	CTCF	chr11:55857340-55857490	A549	lung:	n/a	n/a
37	CTCF	chr11:55857222-55857410	A549	lung:	n/a	chr11:55857306-55857313
38	CTCF	chr11:55856583-55857666	A549	lung:	n/a	chr11:55857306-55857313
39	CTCF	chr11:55987346-55987405	GM20000	blood:	n/a	n/a
40	CTCF	chr11:55871069-55871124	GM13977	blood:	n/a	n/a
41	CTCF	chr11:56035842-56035886	LNCaP	prostate:	n/a	n/a
42	CTCF	chr11:56038545-56038609	Pancreas_OC	pancreas:	n/a	n/a
43	CTCF	chr11:55857280-55857430	Caco-2	colon:	n/a	chr11:55857306-55857313
44	CTCF	chr11:55857275-55857526	A549	lung:	n/a	chr11:55857306-55857313
45	CTCF	chr11:55890080-55890230	GM12866	blood:	n/a	n/a
46	CTCF	chr11:55857315-55857414	K562	blood:	n/a	n/a
47	CTCF	chr11:55857380-55857530	BE2_C	brain:	n/a	n/a
48	CTCF	chr11:55830312-55830375	GM13976	blood:	n/a	n/a
49	CTCF	chr11:55857301-55857439	GM13977	blood:	n/a	chr11:55857306-55857313
50	CTCF	chr11:55857278-55857489	H1-hESC	embryonic stem cell:	n/a	chr11:55857306-55857313

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:55797628-55797678	H1-hESC	embryonic stem cell:	embryo
2	chr11:55797628-55797678	H1-hESC	embryonic stem cell:	embryo
3	chr11:55861503-55861553	AG10803	skin:	n/a
4	chr11:55999683-55999733	AG10803	skin:	n/a
5	chr11:55889797-55889847	HCF	heart:	n/a
6	chr11:55861503-55861553	CMK	blood:	n/a
7	chr11:56018532-56018582	HPAEpiC	pulmonary alveolar:	n/a
8	chr11:55872995-55873045	RPTEC	kidney:	n/a
9	chr11:55861503-55861553	SKMC	muscle:	n/a
10	chr11:55872995-55873045	AG04449	skin:	fetal
11	chr11:55944198-55944248	HRPEpiC	eye:	n/a
12	chr11:55999683-55999733	HUVEC	blood vessel:	n/a
13	chr11:55889658-55889708	SK-N-SH	brain:	n/a
14	chr11:56000287-56000337	HRPEpiC	eye:	n/a
15	chr11:55889808-55889858	HRPEpiC	eye:	n/a
16	chr11:55872478-55872528	RPTEC	kidney:	n/a
17	chr11:55889808-55889858	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:56000287-56000337	GM12878	blood:	n/a
19	chr11:56018532-56018582	ProgFib	skin:	n/a
20	chr11:56020533-56020583	HIPEpiC	eye:	n/a
21	chr11:55927697-55927747	PFSK-1	brain:	n/a
22	chr11:55889797-55889847	T-47D	breast:	n/a
23	chr11:55797626-55797676	HRE	kidney:	n/a
24	chr11:55861503-55861553	HRE	kidney:	n/a
25	chr11:55890274-55890324	MCF-7	breast:	n/a
26	chr11:55890274-55890324	HepG2	liver:	n/a
27	chr11:56018532-56018582	HMEC	breast:	n/a
28	chr11:55944198-55944248	ovcar-3	ovarian:	n/a
29	chr11:55872467-55872517	RPTEC	kidney:	n/a
30	chr11:56018532-56018582	GM12878	blood:	n/a
31	chr11:55861503-55861553	Caco-2	colon:	n/a
32	chr11:55927697-55927747	AG09319	gingival:	n/a
33	chr11:55944198-55944248	HCPEpiC	choroid plexus:	n/a
34	chr11:55999683-55999733	AG09319	gingival:	n/a
35	chr11:55904782-55904832	HCM	heart:	n/a
36	chr11:56018532-56018582	LNCaP	prostate:	n/a
37	chr11:55889797-55889847	HEK293	kidney:	embryo
38	chr11:55872467-55872517	HRPEpiC	eye:	n/a
39	chr11:56000287-56000337	HCF	heart:	n/a
40	chr11:55797628-55797678	HCT-116	colon:	n/a
41	chr11:56020533-56020583	AG04450	lung:	fetal
42	chr11:55999683-55999733	PFSK-1	brain:	n/a
43	chr11:55872478-55872528	BJ	skin:	n/a
44	chr11:55889808-55889858	ECC-1	luminal epithelium:	n/a
45	chr11:56000287-56000337	MCF-7	breast:	n/a
46	chr11:55872882-55872932	HPAEpiC	pulmonary alveolar:	n/a
47	chr11:55889797-55889847	LNCaP	prostate:	n/a
48	chr11:55797626-55797676	HNPCEpiC	eye:	n/a
49	chr11:55890274-55890324	AG09309	skin:	n/a
50	chr11:55796572-55796622	HMEC	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:55861584..55863423-chr11:55907412..55909639,2	K562	blood:
2	chr11:55921059..55923391-chr11:55935211..55936757,2	K562	blood:
3	chr11:56006842..56008897-chr11:56029755..56032217,2	MCF-7	breast:
4	chr11:55957956..55959587-chr11:55962616..55964605,2	K562	blood:
5	chr11:55921059..55923391-chr11:55935211..55936757,2	K562	blood:
6	chr11:55957956..55959587-chr11:55962616..55964605,2	K562	blood:
7	chr11:56006842..56008897-chr11:56029755..56032217,2	MCF-7	breast:
8	chr11:55861584..55863423-chr11:55907412..55909639,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OR5T2-1	chr11:55972601-55973101	NONHSAT021383

Variant related genes	Relation type
OR5J2	TF binding region
OR5BN2P	TF binding region
OR8I4P	TF binding region
OR5J7P	TF binding region
OR8H2	TF binding region
OR8V1P	TF binding region
OR8I2	TF binding region
OR8J3	TF binding region
OR8J2	TF binding region
OR5AQ1P	TF binding region
ENSG00000213604	TF binding region
OR8H3	TF binding region
OR5T3	TF binding region
OR5J1P	TF binding region
OR5AS1	TF binding region
OR5F2P	TF binding region
OR8K5	TF binding region
OR8K4P	TF binding region
OR5T2	TF binding region
OR5BE1P	TF binding region
OR5T1	TF binding region
OR5BN1P	TF binding region
OR5J2	CpG island
OR5BN2P	CpG island
OR8I4P	CpG island
OR5J7P	CpG island
OR8H2	CpG island
OR8V1P	CpG island
OR8I2	CpG island
OR8J3	CpG island
OR8J2	CpG island
OR5AQ1P	CpG island
ENSG00000213604	CpG island
OR8H3	CpG island
OR5T3	CpG island
OR5J1P	CpG island
OR5AS1	CpG island
OR5F2P	CpG island
OR8K5	CpG island
OR8K4P	CpG island
OR5T2	CpG island
OR5BE1P	CpG island
OR5T1	CpG island
OR5BN1P	CpG island

Extended variants
information (count: 1473 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:1473 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146487505	chr11:55783515-55783516	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs7924823	chr11:55783531-55783532	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs58910125	chr11:55783546-55783547	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs114677082	chr11:55783653-55783654	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs554034027	chr11:55783659-55783660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs546493441	chr11:55783706-55783707	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs572704685	chr11:55783709-55783710	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs559309943	chr11:55783718-55783719	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs375009582	chr11:55783719-55783720	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs560386410	chr11:55783727-55783728	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs561619594	chr11:55783734-55783735	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs542951324	chr11:55783765-55783766	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs540681431	chr11:55785716-55785717	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs559254106	chr11:55785780-55785781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs529795584	chr11:55785791-55785792	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs376201996	chr11:55785831-55785832	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs552038252	chr11:55785843-55785844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs142434770	chr11:55785850-55785851	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs115819478	chr11:55785908-55785909	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs190111183	chr11:55785919-55785920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs528740565	chr11:55785924-55785925	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs546724727	chr11:55785925-55785926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs568433361	chr11:55785965-55785966	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs35479698	chr11:55786346-55786347	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs61888545	chr11:55786360-55786361	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs61888546	chr11:55786387-55786388	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs547257816	chr11:55786389-55786390	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs540028014	chr11:55786394-55786395	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534840460	chr11:55787333-55787334	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs546442505	chr11:55787340-55787341	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs568023256	chr11:55787359-55787360	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs187234115	chr11:55787376-55787377	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs369962460	chr11:55787387-55787388	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs371808224	chr11:55787418-55787419	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs532078217	chr11:55787432-55787433	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs562654902	chr11:55787465-55787466	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs535316565	chr11:55787494-55787495	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs556581068	chr11:55787522-55787523	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs1384101	chr11:55793876-55793877	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs372378996	chr11:55793913-55793914	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs6591833	chr11:55793961-55793962	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573953242	chr11:55793981-55793982	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs567325817	chr11:55795105-55795106	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs531826787	chr11:55795136-55795137	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs550308523	chr11:55795139-55795140	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs571850348	chr11:55795152-55795153	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs539310342	chr11:55795189-55795190	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs17600692	chr11:55795228-55795229	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs17600784	chr11:55795718-55795719	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs532695857	chr11:55795746-55795747	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Renal cell carcinoma	18194544	CNVD
Glioblastoma multiforme	21138945	CNVD
Prostate cancer	18632612	CNVD
Esophageal cancer	21851588	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Glioblastoma multiforme	22286061	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
Breast cancer	21364760	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Colorectal cancer	16272173	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:55798200-55798800	Enhancers	Pancreas	Pancrea
2	chr11:55800400-55800600	Enhancers	Pancreas	Pancrea
3	chr11:55822200-55824800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr11:55822600-55822800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr11:55822600-55823600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr11:55822600-55823800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr11:55822800-55824800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr11:55822800-55834000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
9	chr11:55823000-55823800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr11:55823400-55824000	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr11:55823400-55824600	Enhancers	H1 Cell Line	embryonic stem cell
12	chr11:55823400-55825400	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr11:55823600-55824000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
14	chr11:55823800-55824000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr11:55823800-55824400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr11:55823800-55826000	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr11:55824000-55824200	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr11:55824000-55824200	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr11:55824000-55824800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr11:55824000-55825000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
21	chr11:55824200-55824400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr11:55824200-55825000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
23	chr11:55824400-55825200	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr11:55824400-55825200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr11:55824600-55825800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr11:55824800-55826200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr11:55824800-55827200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
28	chr11:55825000-55825200	Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr11:55825000-55825200	Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr11:55825200-55825400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr11:55825200-55826000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr11:55825200-55826200	Weak transcription	HUES48 Cell Line	embryonic stem cell
33	chr11:55825200-55828600	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr11:55825400-55825800	Active TSS	HUES6 Cell Line	embryonic stem cell
35	chr11:55825400-55825800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr11:55825800-55826800	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr11:55825800-55827200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr11:55826000-55826200	Enhancers	H1 Cell Line	embryonic stem cell
39	chr11:55826000-55826400	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr11:55826000-55827600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chr11:55826200-55826400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr11:55826200-55826400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr11:55826400-55827600	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr11:55826800-55828600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr11:55827200-55827800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr11:55827200-55827800	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr11:55827600-55827800	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr11:55827600-55829000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr11:55827800-55828800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr11:55828600-55828800	Enhancers	HUES64 Cell Line	embryonic stem cell

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