Variant report

Variant	nsv584319
Chromosome Location	chr2:212355500-212428192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:195)
CpG islands
(count:184)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:195 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:212363692-212363815	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:212414722-212414939	HepG2	liver:	n/a	chr2:212414816-212414827
3	CEBPB	chr2:212377956-212378135	HepG2	liver:	n/a	chr2:212378026-212378037
4	CEBPB	chr2:212357683-212357979	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:212372106-212372296	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:212375518-212375530	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr2:212357692-212358007	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:212357657-212358022	IMR90	lung:	n/a	n/a
9	CEBPB	chr2:212363575-212363885	H1-hESC	embryonic stem cell:	n/a	chr2:212363681-212363692
10	CEBPB	chr2:212357678-212358005	A549	lung:	n/a	n/a
11	CEBPB	chr2:212363646-212363764	HepG2	liver:	n/a	chr2:212363681-212363692
12	CEBPB	chr2:212355456-212355746	HepG2	liver:	n/a	chr2:212355578-212355589 chr2:212355580-212355591
13	CHD2	chr2:212363638-212363823	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr2:212368683-212368861	MCF-7	breast:	n/a	n/a
15	CTCF	chr2:212368678-212368869	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr2:212368660-212368810	GM12801	blood:	n/a	n/a
17	CTCF	chr2:212368620-212368770	HCT-116	colon:	n/a	n/a
18	CTCF	chr2:212368669-212368870	GM12891	blood:	n/a	n/a
19	CTCF	chr2:212368720-212368870	GM12870	blood:	n/a	n/a
20	CTCF	chr2:212368640-212368790	AoAF	blood vessel:	n/a	n/a
21	CTCF	chr2:212368720-212368870	NHEK	skin:	n/a	n/a
22	CTCF	chr2:212387121-212387172	Medullo	brain:	n/a	n/a
23	CTCF	chr2:212368686-212368842	HepG2	liver:	n/a	n/a
24	CTCF	chr2:212368700-212368850	GM12866	blood:	n/a	n/a
25	CTCF	chr2:212368767-212368820	Medullo	brain:	n/a	n/a
26	CTCF	chr2:212368620-212368770	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr2:212368680-212368830	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr2:212368700-212368850	GM12872	blood:	n/a	n/a
29	CTCF	chr2:212368640-212368790	HPF	lung:	n/a	n/a
30	CTCF	chr2:212368682-212368877	Gliobla	brain:	n/a	n/a
31	CTCF	chr2:212368700-212368850	GM12868	blood:	n/a	n/a
32	CTCF	chr2:212368660-212368810	GM12868	blood:	n/a	n/a
33	CTCF	chr2:212368740-212368890	GM12870	blood:	n/a	n/a
34	CTCF	chr2:212368680-212368830	HPAF	blood vessel:	n/a	n/a
35	CTCF	chr2:212368660-212368863	GM19240	blood:	n/a	n/a
36	CTCF	chr2:212368700-212368850	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr2:212368633-212368869	GM12892	blood:	n/a	n/a
38	CTCF	chr2:212368660-212368810	HVMF	connective:	n/a	n/a
39	CTCF	chr2:212368667-212368875	MCF-7	breast:	n/a	n/a
40	CTCF	chr2:212368740-212368890	GM12865	blood:	n/a	n/a
41	CTCF	chr2:212368713-212368825	GM20000	blood:	n/a	n/a
42	CTCF	chr2:212368720-212368870	AG09309	skin:	n/a	n/a
43	CTCF	chr2:212368720-212368870	SAEC	small airway:	n/a	n/a
44	CTCF	chr2:212368700-212368850	A549	lung:	n/a	n/a
45	CTCF	chr2:212368707-212368832	GM10248	blood:	n/a	n/a
46	CTCF	chr2:212368740-212368890	HRE	kidney:	n/a	n/a
47	CTCF	chr2:212368640-212368790	K562	blood:	n/a	n/a
48	CTCF	chr2:212368700-212368850	HAc	cerebellar:	n/a	n/a
49	CTCF	chr2:212368640-212368790	HMEC	breast:	n/a	n/a
50	CTCF	chr2:212368621-212368821	K562	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212389424-212389474	HAEpiC	amniotic membrane:	n/a
2	chr2:212389424-212389474	HAEpiC	amniotic membrane:	n/a
3	chr2:212388373-212388423	Caco-2	colon:	n/a
4	chr2:212388373-212388423	GM12891	blood:	n/a
5	chr2:212363715-212363765	HMEC	breast:	n/a
6	chr2:212363715-212363765	PrEC	prostate:	n/a
7	chr2:212389424-212389474	AoSMC	blood vessel:	n/a
8	chr2:212363715-212363765	IMR90	lung:	fetal
9	chr2:212388373-212388423	HEEpiC	esophagus:	n/a
10	chr2:212388373-212388423	HAEpiC	amniotic membrane:	n/a
11	chr2:212389424-212389474	HRPEpiC	eye:	n/a
12	chr2:212388373-212388423	HCF	heart:	n/a
13	chr2:212388373-212388423	AG10803	skin:	n/a
14	chr2:212389424-212389474	HPAEpiC	pulmonary alveolar:	n/a
15	chr2:212388373-212388423	MCF10A-Er-Src	breast:	n/a
16	chr2:212388373-212388423	HPAEpiC	pulmonary alveolar:	n/a
17	chr2:212389424-212389474	AG04450	lung:	fetal
18	chr2:212363715-212363765	AG09319	gingival:	n/a
19	chr2:212388373-212388423	AG04449	skin:	fetal
20	chr2:212389424-212389474	HCF	heart:	n/a
21	chr2:212363715-212363765	GM19239	blood:	n/a
22	chr2:212389424-212389474	Jurkat	blood:	n/a
23	chr2:212389424-212389474	SAEC	small airway:	n/a
24	chr2:212389424-212389474	HL-60	blood:	n/a
25	chr2:212363715-212363765	SAEC	small airway:	n/a
26	chr2:212363715-212363765	HCM	heart:	n/a
27	chr2:212389424-212389474	IMR90	lung:	fetal
28	chr2:212363715-212363765	ovcar-3	ovarian:	n/a
29	chr2:212389424-212389474	GM06990	blood:	n/a
30	chr2:212389424-212389474	NH-A	brain:	n/a
31	chr2:212388373-212388423	K562	blood:	n/a
32	chr2:212388373-212388423	AG09319	gingival:	n/a
33	chr2:212363715-212363765	AG09309	skin:	n/a
34	chr2:212363715-212363765	HNPCEpiC	eye:	n/a
35	chr2:212388373-212388423	CMK	blood:	n/a
36	chr2:212389424-212389474	PFSK-1	brain:	n/a
37	chr2:212388373-212388423	HL-60	blood:	n/a
38	chr2:212363715-212363765	NB4	blood:	n/a
39	chr2:212389424-212389474	MCF10A-Er-Src	breast:	n/a
40	chr2:212388373-212388423	SK-N-SH_RA	brain:	n/a
41	chr2:212388373-212388423	HRE	kidney:	n/a
42	chr2:212389424-212389474	HRCEpiC	kidney:	n/a
43	chr2:212388373-212388423	GM12892	blood:	n/a
44	chr2:212388373-212388423	U87	brain:	n/a
45	chr2:212389424-212389474	HCPEpiC	choroid plexus:	n/a
46	chr2:212363715-212363765	BE2_C	brain:	n/a
47	chr2:212363715-212363765	Hela-S3	cervix:	n/a
48	chr2:212388373-212388423	BJ	skin:	n/a
49	chr2:212389424-212389474	BE2_C	brain:	n/a
50	chr2:212388373-212388423	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr2:212288710..212290756-chr2:212380740..212383126,2	MCF-7	breast:
2	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
3	chr1:203274022..203274758-chr2:212363047..212363985,2	MCF-7	breast:
4	chr2:212320246..212322831-chr2:212376794..212379145,2	MCF-7	breast:
5	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
6	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
7	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
8	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
9	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP119	TF binding region
RNA5SP119	CpG island
ENSG00000233791	chromatin interactions
ENSG00000159388	chromatin interactions

Extended variants
information (count: 3129 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3129 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12053361	chr2:212355500-212355501	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs73069182	chr2:212355574-212355575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs185675143	chr2:212355661-212355662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190179512	chr2:212355709-212355710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs567549336	chr2:212355718-212355719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs182405158	chr2:212355778-212355779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs553498673	chr2:212355817-212355818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs12052398	chr2:212355840-212355841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185205924	chr2:212355866-212355867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558721282	chr2:212355888-212355889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575704509	chr2:212355923-212355924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544744750	chr2:212355938-212355939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs76494213	chr2:212355939-212355940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs190938404	chr2:212355971-212355972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62178801	chr2:212355972-212355973	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs560244311	chr2:212355975-212355976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73069185	chr2:212356002-212356003	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs546071555	chr2:212356011-212356012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs562193144	chr2:212356038-212356039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs34777036	chr2:212356093-212356094	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs549500336	chr2:212356096-212356097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547918016	chr2:212356109-212356110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs113090083	chr2:212356224-212356225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184082597	chr2:212356244-212356245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527352578	chr2:212356280-212356281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs4561599	chr2:212356281-212356282	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs189019788	chr2:212356355-212356356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142469156	chr2:212356415-212356416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs552812500	chr2:212356430-212356431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4305210	chr2:212356436-212356437	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs538256647	chr2:212356507-212356508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147917831	chr2:212356630-212356631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs141762244	chr2:212356633-212356634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193022873	chr2:212356680-212356681	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs116296721	chr2:212356730-212356731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576966902	chr2:212356740-212356741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs183048984	chr2:212356777-212356778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs202107699	chr2:212356795-212356796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs386392479	chr2:212356796-212356797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs386392480	chr2:212356805-212356806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs371894577	chr2:212356806-212356807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs548382848	chr2:212356820-212356821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575898396	chr2:212356836-212356837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs562042309	chr2:212356874-212356875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530736951	chr2:212356898-212356899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566691079	chr2:212356923-212356924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112729782	chr2:212356946-212356947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs565147276	chr2:212356959-212356960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534050461	chr2:212356989-212356990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4672615	chr2:212356992-212356993	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:112 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212352800-212362200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr2:212353000-212363400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr2:212358600-212359200	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr2:212358800-212359400	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr2:212359200-212363200	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr2:212359400-212363200	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr2:212362000-212365400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr2:212362200-212362800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:212362200-212364000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr2:212362600-212363800	Enhancers	Brain Angular Gyrus	brain
11	chr2:212362800-212363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr2:212362800-212363800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr2:212362800-212363800	Enhancers	Brain Hippocampus Middle	brain
14	chr2:212362800-212368600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr2:212363200-212363400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:212363200-212363800	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr2:212363200-212363800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr2:212363200-212363800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
19	chr2:212363200-212364000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr2:212363200-212364000	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr2:212363200-212364000	Enhancers	Brain Cingulate Gyrus	brain
22	chr2:212363200-212364000	Enhancers	Brain Substantia Nigra	brain
23	chr2:212363400-212363600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
24	chr2:212363400-212363800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:212363400-212363800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
26	chr2:212363400-212363800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr2:212363400-212363800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
28	chr2:212363400-212364000	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:212363600-212363800	Flanking Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr2:212363800-212364000	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr2:212363800-212364000	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:212364000-212364400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:212364000-212364400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr2:212364400-212364800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr2:212364400-212365200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr2:212364600-212365400	Enhancers	Fetal Heart	heart
37	chr2:212367800-212368200	ZNF genes & repeats	Aorta	Aorta
38	chr2:212368600-212368800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr2:212368600-212369400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:212369400-212377600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr2:212374400-212375200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr2:212374400-212375200	Enhancers	Brain Substantia Nigra	brain
43	chr2:212374600-212375000	Enhancers	Brain Hippocampus Middle	brain
44	chr2:212374600-212377600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:212375000-212377400	Weak transcription	Brain Hippocampus Middle	brain
46	chr2:212376400-212377600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr2:212376800-212377800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr2:212377000-212378400	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr2:212377400-212377600	Enhancers	Fetal Kidney	kidney
50	chr2:212377400-212377800	Enhancers	HUES6 Cell Line	embryonic stem cell

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