Variant report

Variant	nsv970839
Chromosome Location	chr7:56183660-56196274
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:24)
CpG islands
(count:488)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr7:56183720-56183870	SK-N-SH_RA	brain:	n/a	n/a
2	EGR1	chr7:56189203-56189424	K562	blood:	n/a	n/a
3	EGR1	chr7:56189229-56189451	K562	blood:	n/a	n/a
4	ELF1	chr7:56193586-56193799	K562	blood:	n/a	n/a
5	ELF1	chr7:56189165-56189486	K562	blood:	n/a	chr7:56189311-56189324
6	FOSL1	chr7:56189198-56189518	K562	blood:	n/a	n/a
7	GATA2	chr7:56195295-56195408	SH-SY5Y	brain:	n/a	n/a
8	IRF1	chr7:56193269-56193751	K562	blood:	n/a	chr7:56193700-56193717 chr7:56193702-56193715 chr7:56193702-56193713 chr7:56193700-56193714 chr7:56193701-56193715 chr7:56193349-56193361
9	IRF1	chr7:56193389-56194021	K562	blood:	n/a	chr7:56193700-56193717 chr7:56193702-56193715 chr7:56193702-56193713 chr7:56193700-56193714 chr7:56193701-56193715
10	JUN	chr7:56192236-56192474	HepG2	liver:	n/a	n/a
11	JUN	chr7:56189052-56189498	K562	blood:	n/a	n/a
12	JUND	chr7:56189207-56189403	HepG2	liver:	n/a	chr7:56189322-56189333
13	JUND	chr7:56189163-56189498	K562	blood:	n/a	chr7:56189322-56189333
14	JUND	chr7:56192342-56192408	K562	blood:	n/a	n/a
15	JUND	chr7:56192202-56192567	HepG2	liver:	n/a	n/a
16	MAZ	chr7:56193692-56193706	HepG2	liver:	n/a	n/a
17	MYC	chr7:56191660-56191825	H1-hESC	embryonic stem cell:	n/a	n/a
18	POLR2A	chr7:56193806-56193853	GM12878	blood:	n/a	n/a
19	POLR2A	chr7:56184324-56184400	MCF-7	breast:	n/a	n/a
20	POLR2A	chr7:56189894-56190028	H1-hESC	embryonic stem cell:	n/a	n/a
21	RCOR1	chr7:56189169-56189438	K562	blood:	n/a	n/a
22	RCOR1	chr7:56191699-56191786	Hela-S3	cervix:	n/a	n/a
23	TBL1XR1	chr7:56185529-56185593	K562	blood:	n/a	n/a
24	ZNF384	chr7:56195392-56195567	K562	blood:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:56184054-56184104	AG04450	lung:	fetal
2	chr7:56185143-56185193	Hepatocyte	liver:	n/a
3	chr7:56184866-56184916	SK-N-SH_RA	brain:	n/a
4	chr7:56184217-56184267	HNPCEpiC	eye:	n/a
5	chr7:56184217-56184267	IMR90	lung:	fetal
6	chr7:56184153-56184203	SK-N-MC	brain:	n/a
7	chr7:56184153-56184203	Caco-2	colon:	n/a
8	chr7:56184866-56184916	NB4	blood:	n/a
9	chr7:56184217-56184267	HCT-116	colon:	n/a
10	chr7:56184153-56184203	BE2_C	brain:	n/a
11	chr7:56183885-56183935	HPAEpiC	pulmonary alveolar:	n/a
12	chr7:56183885-56183935	AG04450	lung:	fetal
13	chr7:56186623-56186673	HCT-116	colon:	n/a
14	chr7:56183885-56183935	HRCEpiC	kidney:	n/a
15	chr7:56184217-56184267	SAEC	small airway:	n/a
16	chr7:56184217-56184267	GM06990	blood:	n/a
17	chr7:56185143-56185193	HPAEpiC	pulmonary alveolar:	n/a
18	chr7:56184054-56184104	HCF	heart:	n/a
19	chr7:56186623-56186673	K562	blood:	n/a
20	chr7:56186623-56186673	HEK293	kidney:	embryo
21	chr7:56184866-56184916	HAEpiC	amniotic membrane:	n/a
22	chr7:56183885-56183935	AG10803	skin:	n/a
23	chr7:56184054-56184104	HUVEC	blood vessel:	n/a
24	chr7:56184866-56184916	LNCaP	prostate:	n/a
25	chr7:56184866-56184916	HCM	heart:	n/a
26	chr7:56183885-56183935	GM19239	blood:	n/a
27	chr7:56184866-56184916	NHBE	bronchial:	n/a
28	chr7:56186623-56186673	RPTEC	kidney:	n/a
29	chr7:56185143-56185193	AG04450	lung:	fetal
30	chr7:56183885-56183935	AG09319	gingival:	n/a
31	chr7:56186623-56186673	A549	lung:	n/a
32	chr7:56184054-56184104	BJ	skin:	n/a
33	chr7:56184217-56184267	HCF	heart:	n/a
34	chr7:56186623-56186673	HMEC	breast:	n/a
35	chr7:56185143-56185193	AG09309	skin:	n/a
36	chr7:56185143-56185193	Caco-2	colon:	n/a
37	chr7:56184866-56184916	Jurkat	blood:	n/a
38	chr7:56184217-56184267	HRE	kidney:	n/a
39	chr7:56183885-56183935	GM12878	blood:	n/a
40	chr7:56186623-56186673	GM06990	blood:	n/a
41	chr7:56184153-56184203	AG04449	skin:	fetal
42	chr7:56185398-56185448	HL-60	blood:	n/a
43	chr7:56186623-56186673	AoSMC	blood vessel:	n/a
44	chr7:56185398-56185448	AoSMC	blood vessel:	n/a
45	chr7:56185143-56185193	NHBE	bronchial:	n/a
46	chr7:56184866-56184916	SAEC	small airway:	n/a
47	chr7:56185398-56185448	A549	lung:	n/a
48	chr7:56185398-56185448	Caco-2	colon:	n/a
49	chr7:56186623-56186673	SK-N-MC	brain:	n/a
50	chr7:56184054-56184104	MCF10A-Er-Src	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr7:56185532..56188075-chr7:56191363..56193992,2	K562	blood:
2	chr7:56185532..56188075-chr7:56191363..56193992,2	K562	blood:
3	chr7:56182829..56185500-chr7:56187220..56189290,2	K562	blood:

No data

Variant related genes	Relation type
NUPR1L	TF binding region
NUPR1L	CpG island
ENSG00000185290	chromatin interactions

Extended variants
information (count: 350 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:350 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530572577	chr7:56183673-56183674	ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs537880339	chr7:56183776-56183777	ZNF genes & repeats Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs556178084	chr7:56183820-56183821	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs114506539	chr7:56183831-56183832	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs536120059	chr7:56183865-56183866	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs190448728	chr7:56183895-56183896	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs115069654	chr7:56183909-56183910	ZNF genes & repeats Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs13234467	chr7:56184122-56184123	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs116764891	chr7:56184126-56184127	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144082795	chr7:56184164-56184165	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs2270246	chr7:56184174-56184175	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs543448250	chr7:56184183-56184184	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs139443289	chr7:56184222-56184223	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs561727064	chr7:56184223-56184224	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs529958926	chr7:56184229-56184230	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs77155026	chr7:56184235-56184236	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs933466	chr7:56184241-56184242	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs561107324	chr7:56184249-56184250	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs62459297	chr7:56184271-56184272	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs552390932	chr7:56184306-56184307	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs570595378	chr7:56184353-56184354	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs2016482	chr7:56184364-56184365	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs549822822	chr7:56184382-56184383	ZNF genes & repeats Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs371080025	chr7:56184418-56184419	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs569966495	chr7:56184426-56184427	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs532545882	chr7:56184471-56184472	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs535784497	chr7:56184483-56184484	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs2270244	chr7:56184492-56184493	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs566240687	chr7:56184504-56184505	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs539687657	chr7:56184513-56184514	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs149189805	chr7:56184529-56184530	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs368781975	chr7:56184541-56184542	Enhancers Bivalent/Poised TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs374857158	chr7:56184874-56184875	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
34	rs34076765	chr7:56184876-56184877	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs528930529	chr7:56184914-56184915	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
36	rs555874534	chr7:56185144-56185145	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
37	rs536750112	chr7:56185170-56185171	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
38	rs535052052	chr7:56185399-56185400	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
39	rs572391666	chr7:56185543-56185544	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs141205468	chr7:56185568-56185569	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532808424	chr7:56186623-56186624	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs544594009	chr7:56186624-56186625	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
43	rs539078642	chr7:56187221-56187222	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs574526310	chr7:56187248-56187249	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs557377851	chr7:56187258-56187259	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs543296754	chr7:56187269-56187270	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs188978649	chr7:56187272-56187273	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs860117	chr7:56187291-56187292	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs555556504	chr7:56187302-56187303	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs191946593	chr7:56187331-56187332	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Wilms tumour	21544195	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	CNVD
Medulloblastoma	21979893	CNVD
Oligodendroglial tumors	17285580	CNVD
Oral cancer	21386901	CNVD
colon cancer	17210682	CNVD
Lung adenocarcinoma	21810691	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Colorectal cancer	19359472	CNVD
Hypothalamic hamartomas	18252217	CNVD
Human rectal carcinomas	16397240	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Medulloblastoma	18056178	CNVD
Basal cell lymphoma	17170743	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	CNVD
Biliary cancer	19435499	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
Williams-beuren syndrome	22470819	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21750150	CNVD
Hepatocellular carcinoma	16750200	CNVD
Non-small cell lung cancer	21829676	CNVD
Gastric cancer	24379144	CNVD
Glioblastoma multiforme	17002787	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Esophageal cancer	21851588	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Lissencephaly	21572526	CNVD
Breast cancer	17603634	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	16864856	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Glioblastoma multiforme	22291905	CNVD
Glioblastoma multiforme	19435819	CNVD
Intracranial ependymoma	16609018	CNVD
Lung cancer	21911935	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	19455253	CNVD
Lung cancer	17925434	CNVD
Glioma	24330732	CNVD
Lung adenocarcinoma	23938291	CNVD
Glioma	17634744	CNVD
Oral squamous cell carcinoma	19276369	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Lung cancer	20031968	CNVD
Glioblastoma	17090523	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Glioma	17123091	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Medullary thyroid carcinoma	18765511	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:56183400-56184000	Active TSS	Breast Myoepithelial Primary Cells	Breast
2	chr7:56183400-56184000	Bivalent/Poised TSS	Fetal Stomach	stomach
3	chr7:56183400-56184200	Active TSS	Rectal Mucosa Donor 29	rectum
4	chr7:56183400-56184400	Active TSS	Pancreatic Islets	Pancreatic Islet
5	chr7:56183600-56183800	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
7	chr7:56183600-56183800	Bivalent/Poised TSS	Primary hematopoietic stem cells short term culture	blood
8	chr7:56183600-56183800	Bivalent/Poised TSS	Primary T helper cells PMA-I stimulated	--
9	chr7:56183600-56183800	Bivalent/Poised TSS	Primary T helper cells fromperipheralblood	blood
10	chr7:56183600-56183800	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:56183600-56183800	Bivalent/Poised TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr7:56183600-56183800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Brain Germinal Matrix	brain
15	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Colonic Mucosa	Colon
16	chr7:56183600-56183800	Bivalent Enhancer	Colon Smooth Muscle	Colon
17	chr7:56183600-56183800	Flanking Active TSS	Esophagus	oesophagus
18	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Fetal Brain Female	brain
19	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
20	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Fetal Muscle Leg	muscle
21	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Placenta	Placenta
22	chr7:56183600-56183800	Bivalent/Poised TSS	Fetal Thymus	thymus
23	chr7:56183600-56183800	Enhancers	Gastric	stomach
24	chr7:56183600-56183800	Bivalent Enhancer	Lung	lung
25	chr7:56183600-56183800	Bivalent Enhancer	Placenta Amnion	Placenta Amnion
26	chr7:56183600-56183800	Active TSS	Rectal Smooth Muscle	rectum
27	chr7:56183600-56183800	Bivalent Enhancer	Right Atrium	heart
28	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Right Ventricle	heart
29	chr7:56183600-56183800	Flanking Bivalent TSS/Enh	Stomach Mucosa	stomach
30	chr7:56183600-56184000	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
31	chr7:56183600-56184000	Flanking Bivalent TSS/Enh	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr7:56183600-56184000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr7:56183600-56184000	Bivalent/Poised TSS	Primary mononuclear cells fromperipheralblood	Blood
34	chr7:56183600-56184000	Flanking Bivalent TSS/Enh	Brain Cingulate Gyrus	brain
35	chr7:56183600-56184000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
36	chr7:56183600-56184000	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
37	chr7:56183600-56184000	Bivalent Enhancer	Fetal Brain Male	brain
38	chr7:56183600-56184000	Bivalent/Poised TSS	Fetal Intestine Large	intestine
39	chr7:56183600-56184000	Bivalent Enhancer	Ovary	ovary
40	chr7:56183600-56184000	Flanking Active TSS	Psoas Muscle	Psoas
41	chr7:56183600-56184000	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr7:56183600-56184000	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
43	chr7:56183600-56184000	Flanking Active TSS	HMEC	breast
44	chr7:56183600-56184000	Active TSS	HSMM	muscle
45	chr7:56183600-56184200	Bivalent/Poised TSS	Primary hematopoietic stem cells	blood
46	chr7:56183600-56184200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr7:56183600-56184200	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr7:56183600-56184200	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr7:56183600-56184200	Active TSS	Aorta	Aorta
50	chr7:56183600-56184200	Bivalent/Poised TSS	Brain Anterior Caudate	brain

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