Variant report

Variant	esv3350621
Chromosome Location	chr1:209848656-209849030
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:209848445-209848710	K562	blood:	n/a	n/a
2	ATF1	chr1:209848527-209848889	K562	blood:	n/a	n/a
3	BHLHE40	chr1:209848177-209849684	K562	blood:	n/a	chr1:209848854-209848870
4	BHLHE40	chr1:209848397-209848773	GM12878	blood:	n/a	n/a
5	CCNT2	chr1:209848313-209849504	K562	blood:	n/a	n/a
6	CHD2	chr1:209848420-209848861	GM12878	blood:	n/a	n/a
7	CTBP2	chr1:209848410-209849491	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr1:209848900-209849050	HCPEpiC	choroid plexus:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
9	CTCF	chr1:209848860-209849010	HBMEC	blood vessel:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
10	CTCF	chr1:209848900-209849050	Caco-2	colon:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
11	CTCF	chr1:209848900-209849050	HPAF	blood vessel:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
12	CTCF	chr1:209848780-209848930	HCM	heart:	n/a	chr1:209848866-209848879
13	CTCF	chr1:209848880-209849030	HPF	lung:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
14	CTCF	chr1:209848900-209849050	HFF	foreskin:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
15	CTCF	chr1:209848880-209849030	AG04449	skin:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
16	CTCF	chr1:209848920-209849070	SK-N-SH_RA	brain:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
17	CTCF	chr1:209848975-209848999	H1-hESC	embryonic stem cell:	n/a	chr1:209848991-209848999
18	CTCF	chr1:209848980-209849250	WERI-Rb-1	eye:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
19	CTCF	chr1:209849020-209849170	SAEC	small airway:	n/a	n/a
20	CTCF	chr1:209848960-209849110	AoAF	blood vessel:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
21	CTCF	chr1:209848860-209849010	GM12875	blood:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
22	CTCF	chr1:209848920-209849070	AG09309	skin:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
23	CTCF	chr1:209848820-209848970	BJ	skin:	n/a	chr1:209848866-209848879
24	CTCF	chr1:209848960-209849110	HCPEpiC	choroid plexus:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
25	CTCF	chr1:209848928-209848936	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr1:209848720-209849010	AG04449	skin:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
27	CTCF	chr1:209848943-209848957	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr1:209848940-209849190	HEEpiC	esophagus:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
29	CTCF	chr1:209848960-209849110	AG09319	gingival:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
30	CTCF	chr1:209848940-209849090	SAEC	small airway:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
31	CTCF	chr1:209848762-209849434	K562	blood:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
32	CTCF	chr1:209848920-209849070	HCFaa	heart:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
33	CTCF	chr1:209848860-209849010	HA-sp	spinal cord:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
34	CTCF	chr1:209848860-209849010	HMEC	breast:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
35	CTCF	chr1:209848860-209849010	Caco-2	colon:	n/a	chr1:209848983-209849001 chr1:209848866-209848879 chr1:209848991-209848999
36	CTCF	chr1:209848960-209849110	AG04450	lung:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
37	CTCF	chr1:209848900-209849050	HepG2	liver:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
38	CTCF	chr1:209849000-209849150	HRE	kidney:	n/a	n/a
39	CTCF	chr1:209848980-209849130	HMF	breast:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
40	CTCF	chr1:209848940-209849090	BE2_C	brain:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
41	CTCF	chr1:209848900-209849050	HEK293	kidney:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
42	CTCF	chr1:209848880-209849030	AoAF	blood vessel:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
43	CTCF	chr1:209848980-209849130	SK-N-SH_RA	brain:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
44	CTCF	chr1:209848740-209848890	HRE	kidney:	n/a	chr1:209848866-209848879
45	CTCF	chr1:209848900-209849050	AG09319	gingival:	n/a	chr1:209848983-209849001 chr1:209848991-209848999
46	CUX1	chr1:209848155-209848803	K562	blood:	n/a	n/a
47	E2F6	chr1:209848209-209849579	K562	blood:	n/a	chr1:209849000-209849012
48	E2F6	chr1:209848465-209848784	A549	lung:	n/a	n/a
49	E2F6	chr1:209848296-209848785	A549	lung:	n/a	n/a
50	E2F6	chr1:209848890-209849656	H1-hESC	embryonic stem cell:	n/a	chr1:209849000-209849012

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:209849006-209849056	GM19239	blood:	n/a
2	chr1:209848864-209848914	SK-N-SH	brain:	n/a
3	chr1:209848901-209848951	SAEC	small airway:	n/a
4	chr1:209848845-209848895	ECC-1	luminal epithelium:	n/a
5	chr1:209848901-209848951	HepG2	liver:	n/a
6	chr1:209849006-209849056	SK-N-SH	brain:	n/a
7	chr1:209848845-209848895	HRCEpiC	kidney:	n/a
8	chr1:209848901-209848951	ECC-1	luminal epithelium:	n/a
9	chr1:209849006-209849056	SK-N-MC	brain:	n/a
10	chr1:209848864-209848914	HCF	heart:	n/a
11	chr1:209848864-209848914	SK-N-MC	brain:	n/a
12	chr1:209848901-209848951	AG10803	skin:	n/a
13	chr1:209848901-209848951	GM12892	blood:	n/a
14	chr1:209848864-209848914	ECC-1	luminal epithelium:	n/a
15	chr1:209848901-209848951	H1-hESC	embryonic stem cell:	embryo
16	chr1:209848864-209848914	HRPEpiC	eye:	n/a
17	chr1:209848901-209848951	LNCaP	prostate:	n/a
18	chr1:209848845-209848895	H1-hESC	embryonic stem cell:	embryo
19	chr1:209848845-209848895	IMR90	lung:	fetal
20	chr1:209848901-209848951	HCF	heart:	n/a
21	chr1:209848845-209848895	HepG2	liver:	n/a
22	chr1:209848845-209848895	PANC-1	pancreas:	n/a
23	chr1:209848864-209848914	HL-60	blood:	n/a
24	chr1:209849006-209849056	PrEC	prostate:	n/a
25	chr1:209849006-209849056	K562	blood:	n/a
26	chr1:209848901-209848951	Hepatocyte	liver:	n/a
27	chr1:209848864-209848914	GM12891	blood:	n/a
28	chr1:209848845-209848895	HUVEC	blood vessel:	n/a
29	chr1:209848845-209848895	AG09309	skin:	n/a
30	chr1:209848845-209848895	AG04450	lung:	fetal
31	chr1:209849006-209849056	AG09319	gingival:	n/a
32	chr1:209849006-209849056	ECC-1	luminal epithelium:	n/a
33	chr1:209848901-209848951	HIPEpiC	eye:	n/a
34	chr1:209848864-209848914	HRCEpiC	kidney:	n/a
35	chr1:209848901-209848951	Jurkat	blood:	n/a
36	chr1:209848901-209848951	SKMC	muscle:	n/a
37	chr1:209848845-209848895	U87	brain:	n/a
38	chr1:209848901-209848951	T-47D	breast:	n/a
39	chr1:209848901-209848951	HNPCEpiC	eye:	n/a
40	chr1:209848901-209848951	HRCEpiC	kidney:	n/a
41	chr1:209849006-209849056	ProgFib	skin:	n/a
42	chr1:209848864-209848914	HCPEpiC	choroid plexus:	n/a
43	chr1:209848845-209848895	GM06990	blood:	n/a
44	chr1:209848901-209848951	K562	blood:	n/a
45	chr1:209848901-209848951	HL-60	blood:	n/a
46	chr1:209849006-209849056	AG10803	skin:	n/a
47	chr1:209848864-209848914	GM19239	blood:	n/a
48	chr1:209848864-209848914	GM12878	blood:	n/a
49	chr1:209848901-209848951	HCM	heart:	n/a
50	chr1:209848901-209848951	HEK293	kidney:	embryo

Variant related genes	Relation type
G0S2	TF binding region
ENSG00000227591	TF binding region
G0S2	CpG island
ENSG00000227591	CpG island

Extended variants
information (count: 19 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:19 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373701184	chr1:209848656-209848657	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs552079737	chr1:209848686-209848687	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs932375	chr1:209848696-209848697	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs532821821	chr1:209848697-209848698	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs546567604	chr1:209848715-209848716	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs370602402	chr1:209848746-209848747	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs371085022	chr1:209848758-209848759	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs566701786	chr1:209848818-209848819	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs144655136	chr1:209848833-209848834	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs535547227	chr1:209848835-209848836	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs148090379	chr1:209848839-209848840	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs11542711	chr1:209848853-209848854	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs546499183	chr1:209848862-209848863	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs77090413	chr1:209848897-209848898	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs190583758	chr1:209848915-209848916	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs112753859	chr1:209848949-209848950	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs116289160	chr1:209848971-209848972	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs562119503	chr1:209848982-209848983	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs3817870	chr1:209849002-209849003	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:89)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21611746	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD

Chromatin state (count:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209846400-209848800	Enhancers	Spleen	Spleen
2	chr1:209847000-209850000	Flanking Active TSS	Adipose Nuclei	Adipose
3	chr1:209847200-209848800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:209847400-209850000	Flanking Active TSS	Duodenum Mucosa	Duodenum
5	chr1:209847400-209850600	Flanking Active TSS	Liver	Liver
6	chr1:209847600-209849200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
7	chr1:209847600-209849600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
8	chr1:209847600-209850000	Active TSS	Rectal Smooth Muscle	rectum
9	chr1:209847800-209849400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
10	chr1:209847800-209850200	Active TSS	Psoas Muscle	Psoas
11	chr1:209848000-209849000	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:209848000-209849400	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
13	chr1:209848000-209849400	Active TSS	Brain Inferior Temporal Lobe	brain
14	chr1:209848000-209849600	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
15	chr1:209848000-209849600	Flanking Active TSS	Rectal Mucosa Donor 31	rectum
16	chr1:209848000-209849800	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr1:209848000-209849800	Active TSS	Pancreatic Islets	Pancreatic Islet
18	chr1:209848200-209848800	Bivalent Enhancer	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr1:209848200-209848800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr1:209848200-209849000	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
21	chr1:209848200-209849000	Flanking Bivalent TSS/Enh	Primary T cells from cord blood	blood
22	chr1:209848200-209849000	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr1:209848200-209849000	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
24	chr1:209848200-209849000	Active TSS	Fetal Lung	lung
25	chr1:209848200-209849200	Bivalent/Poised TSS	Fetal Brain Female	brain
26	chr1:209848200-209849400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
27	chr1:209848200-209849400	Bivalent/Poised TSS	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr1:209848200-209849400	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
29	chr1:209848200-209849400	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
30	chr1:209848200-209849400	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
31	chr1:209848200-209849400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
32	chr1:209848200-209849400	Active TSS	Fetal Kidney	kidney
33	chr1:209848200-209849400	Flanking Active TSS	Stomach Mucosa	stomach
34	chr1:209848200-209849400	Bivalent/Poised TSS	A549	lung
35	chr1:209848200-209849400	Flanking Active TSS	HMEC	breast
36	chr1:209848200-209849600	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr1:209848200-209849600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
38	chr1:209848200-209849600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr1:209848200-209849600	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
40	chr1:209848200-209849600	Flanking Active TSS	Ovary	ovary
41	chr1:209848200-209849600	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
42	chr1:209848200-209849800	Active TSS	Brain Cingulate Gyrus	brain
43	chr1:209848200-209849800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
44	chr1:209848400-209848800	Bivalent Enhancer	Primary B cells from cord blood	blood
45	chr1:209848400-209848800	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
46	chr1:209848400-209848800	Bivalent Enhancer	Primary T killer naive cells fromperipheralblood	blood
47	chr1:209848400-209848800	Bivalent Enhancer	Fetal Brain Male	brain
48	chr1:209848400-209848800	Flanking Bivalent TSS/Enh	Fetal Stomach	stomach
49	chr1:209848400-209848800	Active TSS	HSMM	muscle
50	chr1:209848400-209848800	Flanking Active TSS	Osteobl	bone

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