Variant report

Variant	nsv999413
Chromosome Location	chr2:49324726-49477527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:405)
CpG islands
(count:305)
Chromatin interactive
region (count:9)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:49467819-49468047	HepG2	liver:	n/a	n/a
2	BACH1	chr2:49367907-49368045	K562	blood:	n/a	n/a
3	BATF	chr2:49368436-49368647	GM12878	blood:	n/a	chr2:49368533-49368544
4	BATF	chr2:49456700-49457056	GM12878	blood:	n/a	n/a
5	BATF	chr2:49456588-49457058	GM12878	blood:	n/a	n/a
6	BCL11A	chr2:49356233-49356526	GM12878	blood:	n/a	n/a
7	BCL11A	chr2:49456707-49457049	GM12878	blood:	n/a	n/a
8	BCL11A	chr2:49456598-49457072	GM12878	blood:	n/a	n/a
9	BCL3	chr2:49475653-49475916	GM12878	blood:	n/a	n/a
10	BHLHE40	chr2:49456686-49457070	HepG2	liver:	n/a	n/a
11	BHLHE40	chr2:49437340-49437444	HepG2	liver:	n/a	n/a
12	BRCA1	chr2:49348882-49348887	GM12878	blood:	n/a	n/a
13	CEBPB	chr2:49381388-49381670	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr2:49426968-49427294	HepG2	liver:	n/a	chr2:49427145-49427158 chr2:49427145-49427156 chr2:49427146-49427157
15	CEBPB	chr2:49389153-49389221	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr2:49468748-49469036	HepG2	liver:	n/a	chr2:49468909-49468922 chr2:49468909-49468920
17	CEBPB	chr2:49475457-49476102	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:49346887-49347087	IMR90	lung:	n/a	chr2:49346959-49346970
19	CEBPB	chr2:49346802-49347083	A549	lung:	n/a	chr2:49346959-49346970
20	CEBPB	chr2:49475560-49476060	A549	lung:	n/a	n/a
21	CEBPB	chr2:49468706-49469063	IMR90	lung:	n/a	chr2:49468909-49468922 chr2:49468909-49468920
22	CEBPB	chr2:49426971-49427266	A549	lung:	n/a	chr2:49427145-49427158 chr2:49427145-49427156 chr2:49427146-49427157
23	CEBPB	chr2:49475606-49475954	A549	lung:	n/a	n/a
24	CEBPB	chr2:49475637-49475993	HepG2	liver:	n/a	n/a
25	CEBPB	chr2:49342728-49342928	HepG2	liver:	n/a	chr2:49342842-49342853
26	CEBPB	chr2:49468771-49469019	A549	lung:	n/a	chr2:49468909-49468922 chr2:49468909-49468920
27	CEBPB	chr2:49475654-49475976	A549	lung:	n/a	n/a
28	CEBPB	chr2:49346807-49347122	HepG2	liver:	n/a	chr2:49346959-49346970
29	CEBPB	chr2:49475649-49476007	Hela-S3	cervix:	n/a	n/a
30	CEBPD	chr2:49456704-49457038	K562	blood:	n/a	n/a
31	CHD2	chr2:49356273-49356541	GM12878	blood:	n/a	n/a
32	CTCF	chr2:49449500-49449650	HFF	foreskin:	n/a	n/a
33	CTCF	chr2:49397440-49397590	GM12874	blood:	n/a	n/a
34	CTCF	chr2:49331387-49331430	GM20000	blood:	n/a	n/a
35	CTCF	chr2:49449500-49449650	RPTEC	kidney:	n/a	n/a
36	CTCF	chr2:49449600-49449750	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr2:49449548-49449642	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:49349420-49349570	GM12867	blood:	n/a	n/a
39	CTCF	chr2:49436400-49436550	HEK293	kidney:	n/a	n/a
40	CTCF	chr2:49449500-49449650	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr2:49449420-49449570	AG04450	lung:	n/a	n/a
42	CTCF	chr2:49449500-49449650	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr2:49356400-49356434	Fibrobl	skin:	n/a	n/a
44	CTCF	chr2:49456902-49456963	Pancreas_OC	pancreas:	n/a	n/a
45	CTCF	chr2:49449467-49449731	IMR90	lung:	n/a	n/a
46	CTCF	chr2:49426100-49426250	GM12867	blood:	n/a	n/a
47	CTCF	chr2:49449557-49449616	ProgFib	skin:	n/a	n/a
48	CTCF	chr2:49350620-49350770	HepG2	liver:	n/a	n/a
49	CTCF	chr2:49449500-49449650	HMEC	breast:	n/a	n/a
50	CTCF	chr2:49437500-49437588	H1-hESC	embryonic stem cell:	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	chr2:49382265-49382315	HRPEpiC	eye:	n/a
2	chr2:49382265-49382315	RPTEC	kidney:	n/a
3	chr2:49382265-49382315	PFSK-1	brain:	n/a
4	chr2:49381495-49381545	SK-N-SH	brain:	n/a
5	chr2:49382159-49382209	Hepatocyte	liver:	n/a
6	chr2:49380959-49381009	A549	lung:	n/a
7	chr2:49381495-49381545	HIPEpiC	eye:	n/a
8	chr2:49380959-49381009	U87	brain:	n/a
9	chr2:49381495-49381545	HL-60	blood:	n/a
10	chr2:49382159-49382209	U87	brain:	n/a
11	chr2:49382401-49382451	CMK	blood:	n/a
12	chr2:49382159-49382209	SK-N-SH_RA	brain:	n/a
13	chr2:49382401-49382451	MCF-7	breast:	n/a
14	chr2:49382401-49382451	SK-N-MC	brain:	n/a
15	chr2:49382265-49382315	GM12878	blood:	n/a
16	chr2:49380959-49381009	IMR90	lung:	fetal
17	chr2:49381495-49381545	GM19239	blood:	n/a
18	chr2:49382401-49382451	GM12891	blood:	n/a
19	chr2:49382401-49382451	HCM	heart:	n/a
20	chr2:49381495-49381545	HRPEpiC	eye:	n/a
21	chr2:49382401-49382451	ECC-1	luminal epithelium:	n/a
22	chr2:49382401-49382451	AG04450	lung:	fetal
23	chr2:49381495-49381545	HNPCEpiC	eye:	n/a
24	chr2:49382265-49382315	H1-hESC	embryonic stem cell:	embryo
25	chr2:49382265-49382315	HepG2	liver:	n/a
26	chr2:49382159-49382209	HIPEpiC	eye:	n/a
27	chr2:49382401-49382451	K562	blood:	n/a
28	chr2:49382265-49382315	HRE	kidney:	n/a
29	chr2:49382159-49382209	NB4	blood:	n/a
30	chr2:49380959-49381009	BE2_C	brain:	n/a
31	chr2:49382159-49382209	AG04449	skin:	fetal
32	chr2:49380959-49381009	HCT-116	colon:	n/a
33	chr2:49381495-49381545	HEK293	kidney:	embryo
34	chr2:49381495-49381545	SKMC	muscle:	n/a
35	chr2:49380959-49381009	HPAEpiC	pulmonary alveolar:	n/a
36	chr2:49381495-49381545	GM06990	blood:	n/a
37	chr2:49381495-49381545	GM12878	blood:	n/a
38	chr2:49382401-49382451	U87	brain:	n/a
39	chr2:49382265-49382315	GM12891	blood:	n/a
40	chr2:49382401-49382451	GM06990	blood:	n/a
41	chr2:49382265-49382315	AoSMC	blood vessel:	n/a
42	chr2:49382159-49382209	GM19239	blood:	n/a
43	chr2:49382159-49382209	SAEC	small airway:	n/a
44	chr2:49382401-49382451	MCF10A-Er-Src	breast:	n/a
45	chr2:49382159-49382209	BE2_C	brain:	n/a
46	chr2:49380959-49381009	H1-hESC	embryonic stem cell:	embryo
47	chr2:49382401-49382451	RPTEC	kidney:	n/a
48	chr2:49382265-49382315	CMK	blood:	n/a
49	chr2:49382159-49382209	Caco-2	colon:	n/a
50	chr2:49380959-49381009	K562	blood:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:49394074..49396341-chr2:49397153..49398810,2	K562	blood:
2	chr2:49467020..49468811-chr2:49494310..49496052,2	MCF-7	breast:
3	chr2:49464339..49466660-chr2:49467162..49469670,2	MCF-7	breast:
4	chr2:49464339..49466660-chr2:49467162..49469670,2	MCF-7	breast:
5	chr2:49476946..49478961-chr2:49480994..49483698,2	K562	blood:
6	chr2:49394074..49396341-chr2:49397153..49398810,2	K562	blood:
7	chr2:49371083..49372770-chr2:49374962..49377778,2	K562	blood:
8	chr2:49371083..49372770-chr2:49374962..49377778,2	K562	blood:
9	chr2:49425509..49426338-chr3:115937869..115938784,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STON1-GTF2A1L-3	chr2:49456719-49457043	NONHSAT070638
2	lnc-STON1-GTF2A1L-3	chr2:49452602-49452611	NONHSAT070638
3	lnc-STON1-GTF2A1L-3	chr2:49437434-49437440	NONHSAT070638
4	lnc-STON1-GTF2A1L-3	chr2:49436966-49437234	NONHSAT070638

No data

Variant related genes	Relation type
FSHR	TF binding region
RNU6-439P	TF binding region
FSHR	CpG island
RNU6-439P	CpG island

Extended variants
information (count: 4056 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:4056 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs75051413	chr2:49324764-49324765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs540616785	chr2:49324814-49324815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559701114	chr2:49324823-49324824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574617141	chr2:49324826-49324827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs72822033	chr2:49324832-49324833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs563299883	chr2:49324845-49324846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561903645	chr2:49324918-49324919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140009531	chr2:49324948-49324949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149869305	chr2:49324958-49324959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569666862	chr2:49325004-49325005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs11898451	chr2:49325023-49325024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs552152800	chr2:49325036-49325037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs11903279	chr2:49325046-49325047	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs3057238	chr2:49325092-49325093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs60395378	chr2:49325093-49325094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs534497552	chr2:49325110-49325111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs1319837	chr2:49325118-49325119	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs529446058	chr2:49325154-49325155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs114487506	chr2:49325197-49325198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1159894	chr2:49325243-49325244	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs2134812	chr2:49325354-49325355	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566930079	chr2:49325386-49325387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186402314	chr2:49325392-49325393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557001521	chr2:49325461-49325462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs144899031	chr2:49325487-49325488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555445954	chr2:49325501-49325502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190941594	chr2:49325507-49325508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs541791227	chr2:49325618-49325619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs575092154	chr2:49325669-49325670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs148626499	chr2:49325695-49325696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374448813	chr2:49325733-49325734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113301654	chr2:49325792-49325793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs550832890	chr2:49325812-49325813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs144356745	chr2:49325818-49325819	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs180756700	chr2:49325825-49325826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs185955963	chr2:49325862-49325863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539860096	chr2:49325887-49325888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs147821154	chr2:49325895-49325896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35014852	chr2:49325900-49325901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs397871549	chr2:49325901-49325902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4638837	chr2:49325948-49325949	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs577633852	chr2:49325958-49325959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551038647	chr2:49325991-49325992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569525208	chr2:49326007-49326008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs143942463	chr2:49326076-49326077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs34255462	chr2:49326077-49326078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533575055	chr2:49326088-49326089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs397870901	chr2:49326095-49326096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551957918	chr2:49326133-49326134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11895457	chr2:49326134-49326135	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:87)

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
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:250 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:49319800-49331800	Weak transcription	Ovary	ovary
2	chr2:49326800-49331000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr2:49331000-49331600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:49331600-49332600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr2:49331800-49333000	Enhancers	Ovary	ovary
6	chr2:49332600-49332800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:49337800-49339000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:49338000-49338600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr2:49338200-49339200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:49338800-49339200	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr2:49349400-49349600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:49349600-49352200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr2:49352200-49352600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr2:49352600-49352800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:49352800-49353400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr2:49353400-49355400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:49355400-49356800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:49355800-49356600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr2:49356600-49356800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
20	chr2:49357400-49357600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr2:49373200-49373400	Enhancers	HSMMtube	muscle
22	chr2:49373800-49374400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:49373800-49376400	Weak transcription	HSMMtube	muscle
24	chr2:49374400-49376400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr2:49376400-49376600	Enhancers	HSMMtube	muscle
26	chr2:49376400-49377200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr2:49376400-49377400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr2:49376400-49377800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr2:49376600-49379800	Weak transcription	HSMMtube	muscle
30	chr2:49377200-49379600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr2:49377400-49380400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr2:49377800-49379400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
33	chr2:49379400-49381800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr2:49379600-49380200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr2:49379800-49380000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr2:49379800-49381200	Flanking Active TSS	HSMMtube	muscle
37	chr2:49380000-49380400	Flanking Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:49380000-49380400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr2:49380000-49380800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr2:49380000-49381200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:49380000-49381200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr2:49380000-49381400	Active TSS	Ovary	ovary
43	chr2:49380000-49382200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr2:49380000-49382200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr2:49380000-49382400	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr2:49380000-49382600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr2:49380200-49380400	Enhancers	H9 Cell Line	embryonic stem cell
48	chr2:49380200-49380400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr2:49380200-49380600	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr2:49380200-49380600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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