Variant report

Variant	nsv979294
Chromosome Location	chr2:114281305-114310836
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:277)
CpG islands
(count:367)
Chromatin interactive
region (count:1)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:277 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr2:114309454-114309460	K562	blood:	n/a	n/a
2	BATF	chr2:114284823-114285271	GM12878	blood:	n/a	chr2:114285118-114285128
3	BATF	chr2:114297909-114298282	GM12878	blood:	n/a	n/a
4	BATF	chr2:114285045-114285287	GM12878	blood:	n/a	chr2:114285118-114285128
5	BATF	chr2:114297986-114298283	GM12878	blood:	n/a	n/a
6	BATF	chr2:114309322-114309698	GM12878	blood:	n/a	chr2:114309606-114309616
7	BATF	chr2:114309258-114309659	GM12878	blood:	n/a	chr2:114309606-114309616
8	BCL11A	chr2:114309351-114309568	GM12878	blood:	n/a	n/a
9	BCL11A	chr2:114309277-114309574	GM12878	blood:	n/a	n/a
10	BCL11A	chr2:114297736-114297986	GM12878	blood:	n/a	n/a
11	BCL11A	chr2:114284936-114285276	GM12878	blood:	n/a	n/a
12	BHLHE40	chr2:114284916-114285249	HepG2	liver:	n/a	n/a
13	CBX3	chr2:114309165-114309826	K562	blood:	n/a	n/a
14	CTCF	chr2:114285220-114285370	BJ	skin:	n/a	n/a
15	CTCF	chr2:114300893-114300939	GM13977	blood:	n/a	n/a
16	CTCF	chr2:114300200-114300350	GM12867	blood:	n/a	n/a
17	CTCF	chr2:114299620-114299910	WERI-Rb-1	eye:	n/a	n/a
18	CTCF	chr2:114299740-114299890	HFF	foreskin:	n/a	n/a
19	CTCF	chr2:114299760-114299910	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr2:114299823-114299880	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chr2:114285220-114285370	AG09319	gingival:	n/a	n/a
22	CTCF	chr2:114299660-114299810	WI-38	lung:	n/a	n/a
23	CTCF	chr2:114299620-114299770	HepG2	liver:	n/a	n/a
24	CTCF	chr2:114299764-114299878	NHEK	skin:	n/a	n/a
25	CTCF	chr2:114285085-114285207	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr2:114285220-114285370	HRE	kidney:	n/a	n/a
27	CTCF	chr2:114299840-114299990	BJ	skin:	n/a	n/a
28	CTCF	chr2:114299702-114299901	Gliobla	brain:	n/a	n/a
29	CTCF	chr2:114299757-114299888	ProgFib	skin:	n/a	n/a
30	CTCF	chr2:114285103-114285276	Gliobla	brain:	n/a	n/a
31	CTCF	chr2:114285864-114285928	MCF-7	breast:	n/a	n/a
32	CTCF	chr2:114309320-114309470	HVMF	connective:	n/a	n/a
33	CTCF	chr2:114285121-114285265	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:114284927-114285347	A549	lung:	n/a	n/a
35	CTCF	chr2:114299690-114299929	A549	lung:	n/a	n/a
36	CTCF	chr2:114285887-114285975	HepG2	liver:	n/a	n/a
37	CTCF	chr2:114285075-114285207	GM13976	blood:	n/a	n/a
38	CTCF	chr2:114285340-114285490	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr2:114284908-114285352	K562	blood:	n/a	n/a
40	CTCF	chr2:114285857-114285942	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:114285034-114285285	LNCaP	prostate:	n/a	n/a
42	CTCF	chr2:114285943-114285967	K562	blood:	n/a	n/a
43	CTCF	chr2:114299826-114299929	Lung_OC	lung:	n/a	n/a
44	CTCF	chr2:114285881-114285948	HepG2	liver:	n/a	n/a
45	CTCF	chr2:114284921-114285379	A549	lung:	n/a	n/a
46	CTCF	chr2:114284954-114285448	A549	lung:	n/a	n/a
47	CTCF	chr2:114309465-114309516	Gliobla	brain:	n/a	n/a
48	CTCF	chr2:114299757-114299872	GM12891	blood:	n/a	n/a
49	CTCF	chr2:114299712-114299910	Fibrobl	skin:	n/a	n/a
50	CTCF	chr2:114299832-114299870	GM10266	blood:	n/a	n/a

(count:367 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:114303932-114303982	HRPEpiC	eye:	n/a
2	chr2:114303932-114303982	HRPEpiC	eye:	n/a
3	chr2:114300610-114300660	HAEpiC	amniotic membrane:	n/a
4	chr2:114299609-114299659	GM12891	blood:	n/a
5	chr2:114300610-114300660	GM12878	blood:	n/a
6	chr2:114299047-114299097	HepG2	liver:	n/a
7	chr2:114299609-114299659	HUVEC	blood vessel:	n/a
8	chr2:114309283-114309333	Jurkat	blood:	n/a
9	chr2:114303932-114303982	NHBE	bronchial:	n/a
10	chr2:114300610-114300660	AG04449	skin:	fetal
11	chr2:114300610-114300660	BJ	skin:	n/a
12	chr2:114303932-114303982	K562	blood:	n/a
13	chr2:114299609-114299659	GM12878	blood:	n/a
14	chr2:114300030-114300080	HAEpiC	amniotic membrane:	n/a
15	chr2:114300610-114300660	CMK	blood:	n/a
16	chr2:114300030-114300080	HepG2	liver:	n/a
17	chr2:114300030-114300080	SAEC	small airway:	n/a
18	chr2:114309283-114309333	BE2_C	brain:	n/a
19	chr2:114299047-114299097	NHDF-neo	bronchial:	n/a
20	chr2:114309283-114309333	LNCaP	prostate:	n/a
21	chr2:114300030-114300080	GM06990	blood:	n/a
22	chr2:114299047-114299097	HEK293	kidney:	embryo
23	chr2:114300610-114300660	HRE	kidney:	n/a
24	chr2:114299047-114299097	PFSK-1	brain:	n/a
25	chr2:114303932-114303982	Hepatocyte	liver:	n/a
26	chr2:114299609-114299659	NHDF-neo	bronchial:	n/a
27	chr2:114299047-114299097	Caco-2	colon:	n/a
28	chr2:114300610-114300660	RPTEC	kidney:	n/a
29	chr2:114303932-114303982	LNCaP	prostate:	n/a
30	chr2:114300030-114300080	Caco-2	colon:	n/a
31	chr2:114309283-114309333	MCF-7	breast:	n/a
32	chr2:114309283-114309333	U87	brain:	n/a
33	chr2:114309283-114309333	AG04450	lung:	fetal
34	chr2:114303932-114303982	PrEC	prostate:	n/a
35	chr2:114309283-114309333	AG04449	skin:	fetal
36	chr2:114300610-114300660	Hela-S3	cervix:	n/a
37	chr2:114299047-114299097	HPAEpiC	pulmonary alveolar:	n/a
38	chr2:114299609-114299659	Hela-S3	cervix:	n/a
39	chr2:114300610-114300660	U87	brain:	n/a
40	chr2:114300610-114300660	GM06990	blood:	n/a
41	chr2:114303932-114303982	GM12878	blood:	n/a
42	chr2:114309283-114309333	GM12878	blood:	n/a
43	chr2:114309283-114309333	HNPCEpiC	eye:	n/a
44	chr2:114309283-114309333	NB4	blood:	n/a
45	chr2:114300610-114300660	K562	blood:	n/a
46	chr2:114299047-114299097	HCM	heart:	n/a
47	chr2:114299609-114299659	AG04450	lung:	fetal
48	chr2:114300030-114300080	BJ	skin:	n/a
49	chr2:114309283-114309333	HRPEpiC	eye:	n/a
50	chr2:114300610-114300660	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:114284812..114285348-chr2:114457736..114458446,2	MCF-7	breast:

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC016745.1-6	chr2:114305096-114305475	NONHSAT073799
2	lnc-AC016745.1-6	chr2:114304899-114305475	l_1930_chr2:114303057-114317403_testes
3	lnc-AC016745.1-1	chr2:114293384-114293576	ENSG00000231943
4	lnc-AC016745.1-6	chr2:114305577-114305635	l_1930_chr2:114303057-114317403_testes
5	lnc-AC016745.1-1	chr2:114300124-114300213	ENSG00000231943
6	lnc-AC016745.1-6	chr2:114303058-114303584	l_1930_chr2:114303057-114317403_testes
7	lnc-AC016745.1-1	chr2:114285145-114285229	ENSG00000231943
8	lnc-AC016745.1-1	chr2:114300124-114300235	ENSG00000231943
9	lnc-AC016745.1-1	chr2:114286497-114286679	ENSG00000231943
10	lnc-AC016745.1-1	chr2:114297629-114298046	ENSG00000231943
11	lnc-AC016745.1-6	chr2:114305235-114305475	NONHSAT073800
12	lnc-AC016745.1-1	chr2:114300124-114300242	ENSG00000231943
13	lnc-AC016745.1-1	chr2:114292137-114292293	ENSG00000231943
14	lnc-AC016745.1-1	chr2:114300124-114300249	ENSG00000231943
15	lnc-AC016745.1-1	chr2:114293384-114293576	ENSG00000231943
16	lnc-AC016745.1-1	chr2:114298727-114298783	ENSG00000231943
17	lnc-AC016745.1-1	chr2:114286224-114286679	ENSG00000231943
18	lnc-AC016745.1-1	chr2:114300124-114300242	ENSG00000231943
19	lnc-AC016745.1-6	chr2:114305577-114305774	NONHSAT073799
20	lnc-AC016745.1-6	chr2:114305577-114305632	NONHSAT073800
21	lnc-AC016745.1-6	chr2:114303437-114303584	NONHSAT073798
22	lnc-AC016745.1-6	chr2:114304899-114305166	NONHSAT073798
23	lnc-AC016745.1-1	chr2:114293384-114293576	ENSG00000231943
24	lnc-AC016745.1-1	chr2:114297633-114298046	ENSG00000231943

No data

Variant related genes	Relation type
ENSG00000225398	TF binding region
ENSG00000231943	TF binding region
ENSG00000225398	CpG island
ENSG00000231943	CpG island

Extended variants
information (count: 295 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:295 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566210124	chr2:114285228-114285229	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs535206989	chr2:114285229-114285230	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs545429510	chr2:114285466-114285467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs552630459	chr2:114285469-114285470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11123192	chr2:114285471-114285472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140735642	chr2:114285509-114285510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73955036	chr2:114285563-114285564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs11123193	chr2:114285568-114285569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201670909	chr2:114285585-114285586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs73955037	chr2:114285716-114285717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182694182	chr2:114285722-114285723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11123194	chr2:114285725-114285726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11123195	chr2:114285733-114285734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556411811	chr2:114285752-114285753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs199936959	chr2:114285753-114285754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs201279147	chr2:114285754-114285755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs202124323	chr2:114285756-114285757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs199947537	chr2:114285757-114285758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs200967357	chr2:114285758-114285759	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112905363	chr2:114285767-114285768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs141038088	chr2:114286323-114286324	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs2260363	chr2:114286331-114286332	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs537667509	chr2:114286360-114286361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs557356282	chr2:114286364-114286365	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs570839853	chr2:114286365-114286366	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs539044390	chr2:114286375-114286376	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs552589243	chr2:114286376-114286377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs144758338	chr2:114286381-114286382	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs541513691	chr2:114286502-114286503	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs1739538	chr2:114286515-114286516	Inactive region	lncRNA	n/a	Overlapped CNVs	mRNA abundance
31	rs79297425	chr2:114286527-114286528	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs116540922	chr2:114286531-114286532	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs543471877	chr2:114286563-114286564	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs564349690	chr2:114286617-114286618	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs199762792	chr2:114292179-114292180	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs199923372	chr2:114292181-114292182	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs565665838	chr2:114294025-114294026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534196077	chr2:114294042-114294043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs547517635	chr2:114294072-114294073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567663181	chr2:114294104-114294105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs536304698	chr2:114294122-114294123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs556718197	chr2:114294140-114294141	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs10169947	chr2:114294156-114294157	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs539268877	chr2:114294168-114294169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs144756146	chr2:114294175-114294176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs10170050	chr2:114294195-114294196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs566275572	chr2:114294208-114294209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201093077	chr2:114294243-114294244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs541012795	chr2:114294276-114294277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs560680869	chr2:114294354-114294355	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Hepatocellular carcinoma	16750200	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
lymphocytic leukemia	21291569	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Colorectal cancer	16272173	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
myoclonus epilepsy	18472482	CNVD
Benign familial neonatal-infantile seizures	18472482	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Colorectal cancer	16912164	CNVD
Ischaemic stroke	16980335	CNVD
Acute myeloid leukemia	18000384	CNVD
Nephronophthisis	17901113	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:230 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:114285400-114285800	Enhancers	Dnd41	blood
2	chr2:114294000-114294400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:114294400-114298600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:114298200-114298600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
5	chr2:114298400-114298600	Enhancers	Fetal Stomach	stomach
6	chr2:114298400-114298600	Enhancers	K562	blood
7	chr2:114298400-114298800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
8	chr2:114298400-114298800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr2:114298400-114298800	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr2:114298400-114299600	Active TSS	Rectal Mucosa Donor 29	rectum
11	chr2:114298400-114300000	Active TSS	HSMMtube	muscle
12	chr2:114298600-114298800	Flanking Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:114298600-114298800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr2:114298600-114298800	Bivalent/Poised TSS	Dnd41	blood
15	chr2:114298600-114299000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
16	chr2:114298600-114299800	Active TSS	Fetal Lung	lung
17	chr2:114298600-114299800	Active TSS	K562	blood
18	chr2:114298600-114300000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr2:114298600-114300600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr2:114298600-114301200	Active TSS	NHLF	lung
21	chr2:114298800-114299000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
22	chr2:114298800-114299000	Bivalent/Poised TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr2:114298800-114299000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr2:114298800-114299000	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:114298800-114299000	Flanking Bivalent TSS/Enh	iPS-18 Cell Line	embryonic stem cell
26	chr2:114298800-114299000	Bivalent/Poised TSS	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:114298800-114299000	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
28	chr2:114298800-114299000	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr2:114298800-114299000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr2:114298800-114299000	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr2:114298800-114299000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr2:114298800-114299000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr2:114298800-114299000	Active TSS	Liver	Liver
34	chr2:114298800-114299000	Active TSS	Skeletal Muscle Male	skeletal muscle
35	chr2:114298800-114299000	Bivalent Enhancer	Stomach Mucosa	stomach
36	chr2:114298800-114299000	Active TSS	Thymus	Thymus
37	chr2:114298800-114299000	Enhancers	Spleen	Spleen
38	chr2:114298800-114299000	Active TSS	HMEC	breast
39	chr2:114298800-114299200	Bivalent/Poised TSS	Primary monocytes fromperipheralblood	blood
40	chr2:114298800-114299200	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
41	chr2:114298800-114299200	Flanking Bivalent TSS/Enh	Cortex derived primary cultured neurospheres	brain
42	chr2:114298800-114299200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
43	chr2:114298800-114299200	Active TSS	Colonic Mucosa	Colon
44	chr2:114298800-114299200	Bivalent/Poised TSS	Fetal Stomach	stomach
45	chr2:114298800-114299400	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr2:114298800-114299400	Flanking Bivalent TSS/Enh	Primary T helper cells fromperipheralblood	blood
47	chr2:114298800-114299400	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
48	chr2:114298800-114299400	Active TSS	Placenta	Placenta
49	chr2:114298800-114299400	Bivalent/Poised TSS	Fetal Thymus	thymus
50	chr2:114298800-114299400	Active TSS	Right Ventricle	heart

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