Variant report

Variant	nsv1006364
Chromosome Location	chr2:49096139-49147372
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:245)
CpG islands
(count:305)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr2:49101542-49101806	A549	lung:	n/a	chr2:49101657-49101668
2	CEBPB	chr2:49101503-49101844	HepG2	liver:	n/a	chr2:49101657-49101668
3	CEBPB	chr2:49101488-49101827	IMR90	lung:	n/a	chr2:49101657-49101668
4	CEBPB	chr2:49101520-49101808	K562	blood:	n/a	chr2:49101657-49101668
5	CEBPB	chr2:49117101-49117221	HepG2	liver:	n/a	n/a
6	CHD2	chr2:49114871-49114923	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr2:49129760-49129910	HAc	cerebellar:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
8	CTCF	chr2:49129820-49129970	BE2_C	brain:	n/a	n/a
9	CTCF	chr2:49129700-49129850	HepG2	liver:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
10	CTCF	chr2:49129680-49129830	GM12872	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
11	CTCF	chr2:49142543-49142628	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr2:49139360-49139510	GM12865	blood:	n/a	n/a
13	CTCF	chr2:49139390-49139523	K562	blood:	n/a	n/a
14	CTCF	chr2:49139240-49139390	RPTEC	kidney:	n/a	n/a
15	CTCF	chr2:49142483-49142681	MCF-7	breast:	n/a	n/a
16	CTCF	chr2:49139280-49139430	A549	lung:	n/a	n/a
17	CTCF	chr2:49139360-49139510	HFF	foreskin:	n/a	n/a
18	CTCF	chr2:49139400-49139550	HCM	heart:	n/a	n/a
19	CTCF	chr2:49139340-49139490	Caco-2	colon:	n/a	n/a
20	CTCF	chr2:49139416-49139461	NHEK	skin:	n/a	n/a
21	CTCF	chr2:49129742-49129871	K562	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
22	CTCF	chr2:49139338-49139524	MCF-7	breast:	n/a	n/a
23	CTCF	chr2:49139340-49139490	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr2:49129660-49129810	HBMEC	blood vessel:	n/a	n/a
25	CTCF	chr2:49129740-49129890	GM12873	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
26	CTCF	chr2:49129760-49129910	NB4	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
27	CTCF	chr2:49129700-49129850	HCPEpiC	choroid plexus:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
28	CTCF	chr2:49129700-49129850	WERI-Rb-1	eye:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
29	CTCF	chr2:49103240-49103390	WERI-Rb-1	eye:	n/a	n/a
30	CTCF	chr2:49142648-49142736	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr2:49141438-49141453	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr2:49139380-49139530	GM12869	blood:	n/a	n/a
33	CTCF	chr2:49129760-49129910	GM12872	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
34	CTCF	chr2:49129840-49129990	GM12864	blood:	n/a	n/a
35	CTCF	chr2:49129600-49129750	HCT-116	colon:	n/a	n/a
36	CTCF	chr2:49100700-49100850	WERI-Rb-1	eye:	n/a	n/a
37	CTCF	chr2:49139340-49139490	GM12875	blood:	n/a	n/a
38	CTCF	chr2:49139376-49139488	GM12878	blood:	n/a	n/a
39	CTCF	chr2:49129680-49129830	Caco-2	colon:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
40	CTCF	chr2:49139306-49139540	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:49139340-49139490	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr2:49139200-49139350	GM06990	blood:	n/a	n/a
43	CTCF	chr2:49129740-49129890	AG04450	lung:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
44	CTCF	chr2:49129780-49129930	AG04450	lung:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
45	CTCF	chr2:49142501-49142613	A549	lung:	n/a	n/a
46	CTCF	chr2:49129740-49129890	GM12866	blood:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
47	CTCF	chr2:49129720-49129870	A549	lung:	n/a	chr2:49129805-49129823 chr2:49129807-49129828
48	CTCF	chr2:49139305-49139563	IMR90	lung:	n/a	n/a
49	CTCF	chr2:49142500-49142650	MCF-7	breast:	n/a	n/a
50	CTCF	chr2:49139382-49139484	Gliobla	brain:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:49143334-49143384	Hepatocyte	liver:	n/a
2	chr2:49143534-49143584	HCT-116	colon:	n/a
3	chr2:49143334-49143384	MCF-7	breast:	n/a
4	chr2:49097906-49097956	IMR90	lung:	fetal
5	chr2:49143534-49143584	AG04450	lung:	fetal
6	chr2:49143534-49143584	SK-N-MC	brain:	n/a
7	chr2:49097906-49097956	HRE	kidney:	n/a
8	chr2:49143334-49143384	AG09319	gingival:	n/a
9	chr2:49143534-49143584	HEEpiC	esophagus:	n/a
10	chr2:49115406-49115456	GM19239	blood:	n/a
11	chr2:49115406-49115456	SAEC	small airway:	n/a
12	chr2:49143334-49143384	NHDF-neo	bronchial:	n/a
13	chr2:49097906-49097956	NT2-D1	testis:	n/a
14	chr2:49097906-49097956	GM19239	blood:	n/a
15	chr2:49143238-49143288	HRPEpiC	eye:	n/a
16	chr2:49115406-49115456	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:49143534-49143584	AG04449	skin:	fetal
18	chr2:49143534-49143584	AG09319	gingival:	n/a
19	chr2:49097906-49097956	RPTEC	kidney:	n/a
20	chr2:49115406-49115456	H1-hESC	embryonic stem cell:	embryo
21	chr2:49143334-49143384	GM12892	blood:	n/a
22	chr2:49143238-49143288	K562	blood:	n/a
23	chr2:49143238-49143288	AG09309	skin:	n/a
24	chr2:49143534-49143584	GM12892	blood:	n/a
25	chr2:49097906-49097956	ovcar-3	ovarian:	n/a
26	chr2:49143334-49143384	CMK	blood:	n/a
27	chr2:49143238-49143288	T-47D	breast:	n/a
28	chr2:49115406-49115456	HepG2	liver:	n/a
29	chr2:49143534-49143584	NH-A	brain:	n/a
30	chr2:49115406-49115456	SK-N-SH	brain:	n/a
31	chr2:49143334-49143384	ECC-1	luminal epithelium:	n/a
32	chr2:49115406-49115456	MCF10A-Er-Src	breast:	n/a
33	chr2:49143238-49143288	PANC-1	pancreas:	n/a
34	chr2:49143334-49143384	AG04450	lung:	fetal
35	chr2:49115406-49115456	HMEC	breast:	n/a
36	chr2:49143238-49143288	ProgFib	skin:	n/a
37	chr2:49115406-49115456	T-47D	breast:	n/a
38	chr2:49115406-49115456	BJ	skin:	n/a
39	chr2:49115406-49115456	NHDF-neo	bronchial:	n/a
40	chr2:49143238-49143288	AoSMC	blood vessel:	n/a
41	chr2:49143334-49143384	HUVEC	blood vessel:	n/a
42	chr2:49143534-49143584	PFSK-1	brain:	n/a
43	chr2:49143238-49143288	HL-60	blood:	n/a
44	chr2:49115406-49115456	HEEpiC	esophagus:	n/a
45	chr2:49143334-49143384	SAEC	small airway:	n/a
46	chr2:49143334-49143384	HRPEpiC	eye:	n/a
47	chr2:49143534-49143584	Hepatocyte	liver:	n/a
48	chr2:49143238-49143288	Hela-S3	cervix:	n/a
49	chr2:49097906-49097956	Jurkat	blood:	n/a
50	chr2:49097906-49097956	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:49127535..49130275-chr2:49154381..49157152,2	MCF-7	breast:
2	chr2:49081319..49083197-chr2:49107259..49109037,2	MCF-7	breast:
3	chr2:49114963..49117141-chr2:49121572..49123521,3	K562	blood:
4	chr2:49108913..49110824-chr2:49114186..49115949,2	MCF-7	breast:
5	chr2:49121216..49123118-chr2:49126253..49127804,2	MCF-7	breast:
6	chr2:49114963..49117141-chr2:49121572..49123521,3	K562	blood:
7	chr2:48993937..48996711-chr2:49125527..49127927,2	MCF-7	breast:
8	chr2:49096223..49098177-chr2:49104222..49106803,2	MCF-7	breast:
9	chr2:49121216..49123118-chr2:49126253..49127804,2	MCF-7	breast:
10	chr2:49139634..49141993-chr2:49154425..49156573,2	K562	blood:
11	chr2:49096223..49098177-chr2:49104222..49106803,2	MCF-7	breast:
12	chr2:49108913..49110824-chr2:49114186..49115949,2	MCF-7	breast:

No data

Variant related genes	Relation type
CTBP2P5	TF binding region
CTBP2P5	CpG island
ENSG00000068781	chromatin interactions

Extended variants
information (count: 1826 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1826 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1558604	chr2:49096139-49096140	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs555942172	chr2:49096187-49096188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs72823285	chr2:49096190-49096191	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs1558603	chr2:49096214-49096215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs571066579	chr2:49096228-49096229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78522985	chr2:49096236-49096237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535073138	chr2:49096261-49096262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190551676	chr2:49096277-49096278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568356693	chr2:49096310-49096311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs553812876	chr2:49096311-49096312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs72823286	chr2:49096312-49096313	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs576257007	chr2:49096328-49096329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs181989366	chr2:49096375-49096376	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187470815	chr2:49096377-49096378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs542644931	chr2:49096380-49096381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs17037685	chr2:49096382-49096383	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs574398048	chr2:49096385-49096386	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs17037688	chr2:49096431-49096432	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs559062142	chr2:49096482-49096483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529640317	chr2:49096484-49096485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs137891149	chr2:49096542-49096543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190617213	chr2:49096565-49096566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs149469041	chr2:49096584-49096585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs375332899	chr2:49096585-49096586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs552907590	chr2:49096595-49096596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143951465	chr2:49096599-49096600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs150195303	chr2:49096649-49096650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35486816	chr2:49096659-49096660	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34682390	chr2:49096664-49096665	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs35457516	chr2:49096698-49096699	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs35751793	chr2:49096730-49096731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs535600092	chr2:49096731-49096732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs180848254	chr2:49096769-49096770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs185457259	chr2:49096832-49096833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs733726	chr2:49096835-49096836	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs12469769	chr2:49096872-49096873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs550013122	chr2:49096880-49096881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs190266731	chr2:49096921-49096922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78812549	chr2:49097002-49097003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147408409	chr2:49097013-49097014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs182824120	chr2:49097032-49097033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571383925	chr2:49097033-49097034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17037700	chr2:49097054-49097055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs113311322	chr2:49097062-49097063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs139735926	chr2:49097127-49097128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77695397	chr2:49097140-49097141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112109512	chr2:49097155-49097156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs112812289	chr2:49097189-49097190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34835719	chr2:49097223-49097224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564807661	chr2:49097227-49097228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20433910	CNVD
Autism	21701786	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Austim spectrum disorder	21302340	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	20553308	CNVD
Autism	22241247	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	22522925	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:49092800-49098200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:49095200-49097600	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr2:49097400-49097600	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr2:49097400-49098400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr2:49097600-49097800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
6	chr2:49097600-49098200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr2:49097600-49098400	Enhancers	Fetal Stomach	stomach
8	chr2:49097600-49098600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr2:49097800-49098000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr2:49097800-49098000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr2:49097800-49098400	Enhancers	Brain Germinal Matrix	brain
12	chr2:49097800-49098600	Enhancers	H9 Cell Line	embryonic stem cell
13	chr2:49098000-49098200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
14	chr2:49098200-49098600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:49098200-49098600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:49098600-49098800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:49099600-49101000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr2:49100600-49101000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr2:49102000-49102200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr2:49107200-49115400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr2:49111000-49112400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr2:49111600-49111800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr2:49112400-49115000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:49114000-49116200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:49114200-49114400	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr2:49114200-49116000	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr2:49114200-49116200	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr2:49114400-49115000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr2:49114800-49116200	Enhancers	H1 Cell Line	embryonic stem cell
30	chr2:49114800-49116200	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr2:49115000-49115600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr2:49115000-49116000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr2:49115200-49116000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr2:49115200-49116000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr2:49115400-49116000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr2:49115400-49116200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr2:49115600-49120200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr2:49116000-49119600	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr2:49116200-49119400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr2:49117400-49117800	Enhancers	Rectal Smooth Muscle	rectum
41	chr2:49117600-49118800	Enhancers	Colon Smooth Muscle	Colon
42	chr2:49119000-49121000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:49119400-49119600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr2:49119600-49120000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:49120200-49121200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr2:49120200-49127200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:49121000-49121200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:49121000-49121200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr2:49126400-49128400	Enhancers	HSMMtube	muscle
50	chr2:49127000-49128200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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