Variant report

Variant	nsv820203
Chromosome Location	chr2:182542727-182543097
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:99)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:99 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr2:182542806-182542959	K562	blood:	n/a	n/a
2	CBX3	chr2:182542726-182543046	K562	blood:	n/a	n/a
3	CEBPB	chr2:182542652-182542926	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD2	chr2:182542858-182543027	HepG2	liver:	n/a	n/a
5	CHD2	chr2:182542715-182543081	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTBP2	chr2:182542573-182543638	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr2:182542720-182542870	HBMEC	blood vessel:	n/a	n/a
8	CTCF	chr2:182542800-182542950	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr2:182542680-182542830	HRE	kidney:	n/a	n/a
10	CTCF	chr2:182542863-182542938	Fibrobl	skin:	n/a	n/a
11	CTCF	chr2:182542800-182542950	HCPEpiC	choroid plexus:	n/a	n/a
12	EP300	chr2:182542720-182542999	H1-hESC	embryonic stem cell:	n/a	n/a
13	FOXP2	chr2:182542676-182543018	SK-N-MC	brain:	n/a	n/a
14	GTF2F1	chr2:182542815-182543051	H1-hESC	embryonic stem cell:	n/a	n/a
15	HCFC1	chr2:182542816-182542939	K562	blood:	n/a	n/a
16	HDAC2	chr2:182542719-182542957	H1-hESC	embryonic stem cell:	n/a	n/a
17	JUND	chr2:182542682-182543001	H1-hESC	embryonic stem cell:	n/a	n/a
18	KAP1	chr2:182542621-182543079	U2OS	brain:	n/a	n/a
19	KAP1	chr2:182542577-182543103	HEK293	kidney:	n/a	n/a
20	MAFK	chr2:182542920-182542936	HepG2	liver:	n/a	n/a
21	MAX	chr2:182542614-182543093	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr2:182542649-182543097	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAX	chr2:182542639-182543121	A549	lung:	n/a	n/a
24	MAX	chr2:182542680-182543009	K562	blood:	n/a	n/a
25	MAZ	chr2:182542758-182543027	K562	blood:	n/a	n/a
26	MXI1	chr2:182542711-182543075	H1-hESC	embryonic stem cell:	n/a	n/a
27	MXI1	chr2:182542904-182542971	K562	blood:	n/a	n/a
28	MXI1	chr2:182542451-182543249	IMR90	lung:	n/a	n/a
29	MYC	chr2:182542755-182542974	H1-hESC	embryonic stem cell:	n/a	n/a
30	MYC	chr2:182542835-182542926	HUVEC	blood vessel:	n/a	n/a
31	POLR2A	chr2:182542949-182542984	H1-hESC	embryonic stem cell:	n/a	n/a
32	POLR2A	chr2:182542757-182543081	MCF-7	breast:	n/a	n/a
33	POLR2A	chr2:182542857-182542938	H1-hESC	embryonic stem cell:	n/a	n/a
34	POLR2A	chr2:182542309-182543016	H1-neurons	neurons:	n/a	n/a
35	POLR2A	chr2:182542649-182543177	H1-neurons	neurons:	n/a	n/a
36	RAD21	chr2:182542716-182543023	H1-hESC	embryonic stem cell:	n/a	n/a
37	RAD21	chr2:182542667-182543101	H1-hESC	embryonic stem cell:	n/a	n/a
38	RCOR1	chr2:182542708-182543065	K562	blood:	n/a	n/a
39	RCOR1	chr2:182542733-182543053	HepG2	liver:	n/a	n/a
40	REST	chr2:182542545-182543300	GM12878	blood:	n/a	n/a
41	REST	chr2:182542376-182543562	HCT-116	colon:	n/a	n/a
42	REST	chr2:182542715-182543012	GM12878	blood:	n/a	n/a
43	REST	chr2:182542440-182543361	H1-neurons	neurons:	n/a	n/a
44	REST	chr2:182542682-182543078	SK-N-SH	brain:	n/a	n/a
45	REST	chr2:182542619-182543257	K562	blood:	n/a	n/a
46	REST	chr2:182542309-182543623	PFSK-1	brain:	n/a	n/a
47	REST	chr2:182542428-182543110	U87	brain:	n/a	n/a
48	REST	chr2:182542463-182543336	MCF-7	breast:	n/a	n/a
49	REST	chr2:182542531-182543244	A549	lung:	n/a	n/a
50	REST	chr2:182542509-182543338	K562	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:182542901-182542951	CMK	blood:	n/a
2	chr2:182542901-182542951	HEEpiC	esophagus:	n/a
3	chr2:182542864-182542914	PrEC	prostate:	n/a
4	chr2:182542901-182542951	BE2_C	brain:	n/a
5	chr2:182542864-182542914	SAEC	small airway:	n/a
6	chr2:182542901-182542951	NH-A	brain:	n/a
7	chr2:182542901-182542951	PFSK-1	brain:	n/a
8	chr2:182542864-182542914	CMK	blood:	n/a
9	chr2:182542901-182542951	U87	brain:	n/a
10	chr2:182542901-182542951	MCF10A-Er-Src	breast:	n/a
11	chr2:182542864-182542914	HepG2	liver:	n/a
12	chr2:182542864-182542914	HCT-116	colon:	n/a
13	chr2:182542864-182542914	HCF	heart:	n/a
14	chr2:182542901-182542951	HNPCEpiC	eye:	n/a
15	chr2:182542864-182542914	HCM	heart:	n/a
16	chr2:182542864-182542914	SK-N-SH_RA	brain:	n/a
17	chr2:182542864-182542914	NH-A	brain:	n/a
18	chr2:182542864-182542914	HNPCEpiC	eye:	n/a
19	chr2:182542864-182542914	PFSK-1	brain:	n/a
20	chr2:182542901-182542951	HMEC	breast:	n/a
21	chr2:182542864-182542914	T-47D	breast:	n/a
22	chr2:182542901-182542951	HCT-116	colon:	n/a
23	chr2:182542864-182542914	HAEpiC	amniotic membrane:	n/a
24	chr2:182542901-182542951	HRCEpiC	kidney:	n/a
25	chr2:182542901-182542951	AG10803	skin:	n/a
26	chr2:182542901-182542951	BJ	skin:	n/a
27	chr2:182542864-182542914	GM12891	blood:	n/a
28	chr2:182542901-182542951	SK-N-SH	brain:	n/a
29	chr2:182542864-182542914	GM19239	blood:	n/a
30	chr2:182542864-182542914	AG04450	lung:	fetal
31	chr2:182542864-182542914	RPTEC	kidney:	n/a
32	chr2:182542901-182542951	AoSMC	blood vessel:	n/a
33	chr2:182542901-182542951	HCF	heart:	n/a
34	chr2:182542864-182542914	NHDF-neo	bronchial:	n/a
35	chr2:182542864-182542914	HMEC	breast:	n/a
36	chr2:182542901-182542951	PANC-1	pancreas:	n/a
37	chr2:182542864-182542914	GM06990	blood:	n/a
38	chr2:182542864-182542914	AG09309	skin:	n/a
39	chr2:182542864-182542914	AoSMC	blood vessel:	n/a
40	chr2:182542864-182542914	BE2_C	brain:	n/a
41	chr2:182542864-182542914	Hepatocyte	liver:	n/a
42	chr2:182542864-182542914	NHBE	bronchial:	n/a
43	chr2:182542901-182542951	GM19239	blood:	n/a
44	chr2:182542864-182542914	BJ	skin:	n/a
45	chr2:182542901-182542951	NHDF-neo	bronchial:	n/a
46	chr2:182542864-182542914	HEK293	kidney:	embryo
47	chr2:182542901-182542951	NHBE	bronchial:	n/a
48	chr2:182542901-182542951	HIPEpiC	eye:	n/a
49	chr2:182542864-182542914	MCF10A-Er-Src	breast:	n/a
50	chr2:182542901-182542951	Caco-2	colon:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:182541170..182543258-chr2:182550470..182553269,2	MCF-7	breast:
2	chr2:182542601..182545361-chr2:182546496..182548838,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000234595	TF binding region
ENSG00000234595	CpG island
ENSG00000234595	chromatin interactions

Extended variants
information (count: 30 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs201777821	chr2:182542727-182542728	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372654587	chr2:182542773-182542774	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115027760	chr2:182542811-182542812	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556602572	chr2:182542822-182542823	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs577169847	chr2:182542823-182542824	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs147634094	chr2:182542830-182542831	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375390710	chr2:182542837-182542838	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs201293992	chr2:182542838-182542839	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs576169853	chr2:182542839-182542840	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs201542440	chr2:182542847-182542848	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115207271	chr2:182542850-182542851	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs561017686	chr2:182542865-182542866	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs145050582	chr2:182542873-182542874	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs201829057	chr2:182542923-182542924	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs201873722	chr2:182542937-182542938	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs34332535	chr2:182542946-182542947	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs387906384	chr2:182542971-182542972	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs201174472	chr2:182542972-182542973	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs560115414	chr2:182542974-182542975	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs142123958	chr2:182542978-182542979	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs200292501	chr2:182542981-182542982	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371912669	chr2:182542985-182542986	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs8192556	chr2:182542998-182542999	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs138301552	chr2:182543016-182543017	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs538415264	chr2:182543033-182543034	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375030401	chr2:182543034-182543035	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs565522208	chr2:182543048-182543049	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs369182691	chr2:182543077-182543078	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs372600079	chr2:182543084-182543085	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs116304177	chr2:182543096-182543097	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:51)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Seminomas	18059402	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
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Sudden cardiac death	19188705	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Mental retardation	21062444	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:182542200-182543800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:182542400-182542800	Bivalent Enhancer	H9 Cell Line	embryonic stem cell
3	chr2:182542400-182542800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
4	chr2:182542400-182542800	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
5	chr2:182542400-182542800	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
6	chr2:182542400-182542800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
7	chr2:182542400-182542800	Flanking Bivalent TSS/Enh	Fetal Intestine Large	intestine
8	chr2:182542400-182542800	Bivalent Enhancer	Lung	lung
9	chr2:182542400-182542800	Enhancers	Spleen	Spleen
10	chr2:182542400-182543200	Flanking Bivalent TSS/Enh	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr2:182542400-182543200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr2:182542400-182543200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr2:182542400-182543400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
14	chr2:182542400-182543400	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr2:182542400-182543400	Bivalent/Poised TSS	Primary T cells from cord blood	blood
16	chr2:182542400-182543400	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
17	chr2:182542400-182543600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:182542400-182543600	Transcr. at gene 5' and 3'	Pancreatic Islets	Pancreatic Islet
19	chr2:182542400-182543600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
20	chr2:182542400-182545000	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr2:182542400-182545400	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
22	chr2:182542400-182546200	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
23	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
24	chr2:182542600-182542800	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr2:182542600-182542800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:182542600-182542800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
27	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr2:182542600-182542800	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
30	chr2:182542600-182542800	Bivalent/Poised TSS	Primary T killer memory cells from peripheral blood	blood
31	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr2:182542600-182542800	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
33	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
35	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	Liver	Liver
36	chr2:182542600-182542800	Bivalent Enhancer	Esophagus	oesophagus
37	chr2:182542600-182542800	Bivalent Enhancer	Fetal Muscle Leg	muscle
38	chr2:182542600-182542800	Bivalent Enhancer	Left Ventricle	heart
39	chr2:182542600-182542800	Bivalent Enhancer	Right Ventricle	heart
40	chr2:182542600-182542800	Bivalent Enhancer	Small Intestine	intestine
41	chr2:182542600-182542800	Flanking Bivalent TSS/Enh	A549	lung
42	chr2:182542600-182542800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
43	chr2:182542600-182542800	Bivalent Enhancer	NHDF-Ad	bronchial
44	chr2:182542600-182543000	Bivalent Enhancer	Fetal Brain Male	brain
45	chr2:182542600-182543000	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
46	chr2:182542600-182543000	Flanking Active TSS	Pancreas	Pancrea
47	chr2:182542600-182543200	Bivalent Enhancer	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr2:182542600-182543200	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr2:182542600-182543200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr2:182542600-182543200	Bivalent Enhancer	Fetal Intestine Small	intestine

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