Variant report

Variant	esv3526812
Chromosome Location	chr7:5111265-5111831
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:489)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr7:5111471-5111492	K562	blood:	n/a	n/a
2	CHD2	chr7:5111539-5111722	K562	blood:	n/a	n/a
3	E2F6	chr7:5111580-5111819	K562	blood:	n/a	n/a
4	EGR1	chr7:5111529-5111779	K562	blood:	n/a	n/a
5	EGR1	chr7:5111512-5111808	K562	blood:	n/a	n/a
6	ELK1	chr7:5111478-5111499	K562	blood:	n/a	n/a
7	FOSL2	chr7:5111226-5111813	HepG2	liver:	n/a	chr7:5111602-5111610
8	HMGN3	chr7:5111428-5111933	K562	blood:	n/a	n/a
9	IRF1	chr7:5111594-5111813	K562	blood:	n/a	chr7:5111629-5111643
10	MAX	chr7:5111400-5111908	K562	blood:	n/a	n/a
11	MAX	chr7:5111613-5111765	K562	blood:	n/a	n/a
12	MAX	chr7:5111361-5112173	ECC-1	luminal epithelium:	n/a	chr7:5111952-5111962
13	MYC	chr7:5111676-5111697	K562	blood:	n/a	n/a
14	MYC	chr7:5111692-5111746	MCF-7	breast:	n/a	n/a
15	NRF1	chr7:5111578-5111789	K562	blood:	n/a	n/a
16	POLR2A	chr7:5110755-5112018	K562	blood:	n/a	n/a
17	POLR2A	chr7:5110963-5111670	PFSK-1	brain:	n/a	n/a
18	POLR2A	chr7:5111357-5111995	ECC-1	luminal epithelium:	n/a	n/a
19	POLR2A	chr7:5111219-5111913	GM12878	blood:	n/a	n/a
20	POLR2A	chr7:5111216-5111627	U87	brain:	n/a	n/a
21	POLR2A	chr7:5111068-5111843	K562	blood:	n/a	n/a
22	POLR2A	chr7:5111084-5111321	HepG2	liver:	n/a	n/a
23	POLR2A	chr7:5111646-5111667	Gliobla	brain:	n/a	n/a
24	POLR2A	chr7:5111506-5111869	HCT-116	colon:	n/a	n/a
25	POLR2A	chr7:5111377-5111827	HL-60	blood:	n/a	n/a
26	POLR2A	chr7:5111487-5111580	A549	lung:	n/a	n/a
27	POLR2A	chr7:5111366-5111804	GM12891	blood:	n/a	n/a
28	POLR2A	chr7:5111238-5111835	PANC-1	pancreas:	n/a	n/a
29	POLR2A	chr7:5111391-5112212	HepG2	liver:	n/a	n/a
30	POLR2A	chr7:5111368-5111809	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr7:5111322-5111727	HepG2	liver:	n/a	n/a
32	POLR2A	chr7:5111503-5111641	ProgFib	skin:	n/a	n/a
33	POLR2A	chr7:5111276-5112004	U87	brain:	n/a	n/a
34	POLR2A	chr7:5111151-5111739	HL-60	blood:	n/a	n/a
35	POLR2A	chr7:5111161-5111979	SK-N-MC	brain:	n/a	n/a
36	POLR2A	chr7:5111341-5112058	GM12878	blood:	n/a	n/a
37	POLR2A	chr7:5111529-5111851	K562	blood:	n/a	n/a
38	POLR2A	chr7:5111362-5112071	GM12878	blood:	n/a	n/a
39	POLR2A	chr7:5111415-5111867	K562	blood:	n/a	n/a
40	POLR2A	chr7:5111405-5111708	GM12878	blood:	n/a	n/a
41	POLR2A	chr7:5111380-5111615	SK-N-SH	brain:	n/a	n/a
42	POLR2A	chr7:5110740-5111842	MCF-7	breast:	n/a	n/a
43	POLR2A	chr7:5111160-5111773	SK-N-SH	brain:	n/a	n/a
44	POLR2A	chr7:5111473-5111768	HCT-116	colon:	n/a	n/a
45	POLR2A	chr7:5111335-5111963	U87	brain:	n/a	n/a
46	POLR2A	chr7:5111136-5111683	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr7:5111273-5112027	ECC-1	luminal epithelium:	n/a	n/a
48	POLR2A	chr7:5111177-5111851	PANC-1	pancreas:	n/a	n/a
49	POLR2A	chr7:5111552-5111685	A549	lung:	n/a	n/a
50	POLR2A	chr7:5111244-5111627	U87	brain:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5111621-5111671	HCM	heart:	n/a
2	chr7:5111621-5111671	HCM	heart:	n/a
3	chr7:5111488-5111538	AG04449	skin:	fetal
4	chr7:5111488-5111538	MCF10A-Er-Src	breast:	n/a
5	chr7:5111548-5111598	AG04449	skin:	fetal
6	chr7:5111548-5111598	HIPEpiC	eye:	n/a
7	chr7:5111488-5111538	GM06990	blood:	n/a
8	chr7:5111669-5111719	Hepatocyte	liver:	n/a
9	chr7:5111488-5111538	AG10803	skin:	n/a
10	chr7:5111635-5111685	HEK293	kidney:	embryo
11	chr7:5111548-5111598	Jurkat	blood:	n/a
12	chr7:5111669-5111719	SK-N-SH	brain:	n/a
13	chr7:5111488-5111538	HCM	heart:	n/a
14	chr7:5111488-5111538	ECC-1	luminal epithelium:	n/a
15	chr7:5111669-5111719	HEK293	kidney:	embryo
16	chr7:5111548-5111598	NB4	blood:	n/a
17	chr7:5111576-5111626	NHDF-neo	bronchial:	n/a
18	chr7:5111621-5111671	SAEC	small airway:	n/a
19	chr7:5111576-5111626	SK-N-SH_RA	brain:	n/a
20	chr7:5111548-5111598	A549	lung:	n/a
21	chr7:5111635-5111685	GM12878	blood:	n/a
22	chr7:5111488-5111538	HL-60	blood:	n/a
23	chr7:5111621-5111671	BJ	skin:	n/a
24	chr7:5111529-5111579	HEEpiC	esophagus:	n/a
25	chr7:5111529-5111579	SK-N-SH	brain:	n/a
26	chr7:5111641-5111691	SK-N-MC	brain:	n/a
27	chr7:5111621-5111671	HAEpiC	amniotic membrane:	n/a
28	chr7:5111669-5111719	SAEC	small airway:	n/a
29	chr7:5111621-5111671	U87	brain:	n/a
30	chr7:5111529-5111579	ovcar-3	ovarian:	n/a
31	chr7:5111529-5111579	AG04449	skin:	fetal
32	chr7:5111529-5111579	A549	lung:	n/a
33	chr7:5111669-5111719	GM12891	blood:	n/a
34	chr7:5111635-5111685	K562	blood:	n/a
35	chr7:5111641-5111691	HAEpiC	amniotic membrane:	n/a
36	chr7:5111488-5111538	SKMC	muscle:	n/a
37	chr7:5111548-5111598	H1-hESC	embryonic stem cell:	embryo
38	chr7:5111548-5111598	AG10803	skin:	n/a
39	chr7:5111641-5111691	AG04449	skin:	fetal
40	chr7:5111548-5111598	NHDF-neo	bronchial:	n/a
41	chr7:5111529-5111579	AG10803	skin:	n/a
42	chr7:5111576-5111626	GM12891	blood:	n/a
43	chr7:5111635-5111685	HepG2	liver:	n/a
44	chr7:5111641-5111691	A549	lung:	n/a
45	chr7:5111621-5111671	RPTEC	kidney:	n/a
46	chr7:5111669-5111719	HEEpiC	esophagus:	n/a
47	chr7:5111548-5111598	Caco-2	colon:	n/a
48	chr7:5111621-5111671	HCT-116	colon:	n/a
49	chr7:5111641-5111691	IMR90	lung:	fetal
50	chr7:5111621-5111671	GM12892	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:5102498..5105723-chr7:5107748..5111413,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RBAK-1	chr7:5111691-5111831	NONHSAT118901
2	lnc-RBAK-1	chr7:5111756-5111831	ENSG00000273313.1

No data

Variant related genes	Relation type
RBAKDN	TF binding region
RBAKDN	CpG island

Extended variants
information (count: 25 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188803499	chr7:5111321-5111322	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs73673296	chr7:5111327-5111328	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs546852661	chr7:5111340-5111341	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs553927569	chr7:5111366-5111367	ZNF genes & repeats Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs114681207	chr7:5111422-5111423	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs538637698	chr7:5111441-5111442	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs12668748	chr7:5111481-5111482	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs568963592	chr7:5111493-5111494	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
9	rs536870523	chr7:5111521-5111522	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
10	rs534275400	chr7:5111558-5111559	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
11	rs554827137	chr7:5111597-5111598	ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Weak transcription	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
12	rs563205074	chr7:5111626-5111627	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
13	rs573367159	chr7:5111627-5111628	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
14	rs534251786	chr7:5111658-5111659	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs372118185	chr7:5111668-5111669	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs143037328	chr7:5111714-5111715	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
17	rs577724276	chr7:5111717-5111718	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
18	rs544974464	chr7:5111720-5111721	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
19	rs559022979	chr7:5111765-5111766	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
20	rs575217983	chr7:5111780-5111781	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
21	rs542695025	chr7:5111781-5111782	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
22	rs560956237	chr7:5111792-5111793	Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Enhancers Flanking Active TSS Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
23	rs190589431	chr7:5111806-5111807	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
24	rs528288074	chr7:5111823-5111824	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
25	rs62444320	chr7:5111830-5111831	ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Lynch syndrome	22585707	CNVD
Follicular lymphoma	20505157	CNVD
Breast cancer	16397240	CNVD
Raine Syndrome	17924334	CNVD
Diffuse large b-cell lymphoma	21266526	CNVD
Melanoma	18172304	CNVD
Sudden cardiac death	19188705	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Glioma	18556773	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Ovarian cancer	22174824	CNVD
Urothelial carcinoma	18382360	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Biliary cancer	19435499	CNVD
Cancer	16751803	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	17387387	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	18923191	CNVD
Glioma	21971842	CNVD
Glioblastoma multiforme	21080181	CNVD
Liposarcoma	21253554	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
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
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Developmental delay	21147756	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Urothelial carcinoma	21177765	CNVD
Glioblastoma multiforme	21525872	CNVD
Bladder cancer	21909424	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21045282	CNVD
Disorders of sex development	21048976	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:104 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5088200-5111400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr7:5095200-5111600	ZNF genes & repeats	Primary T regulatory cells fromperipheralblood	blood
3	chr7:5105400-5111400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:5106800-5111800	Weak transcription	HepG2	liver
5	chr7:5107000-5111400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr7:5107000-5111400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
7	chr7:5107200-5111600	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
8	chr7:5108600-5117400	Weak transcription	Dnd41	blood
9	chr7:5110000-5111400	Weak transcription	Left Ventricle	heart
10	chr7:5110400-5111400	Weak transcription	Pancreas	Pancrea
11	chr7:5110400-5111600	Weak transcription	Ovary	ovary
12	chr7:5110800-5112000	Bivalent/Poised TSS	Primary T cells from cord blood	blood
13	chr7:5111000-5111400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:5111000-5112000	ZNF genes & repeats	Primary neutrophils fromperipheralblood	blood
15	chr7:5111200-5111400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr7:5111200-5111400	Enhancers	K562	blood
17	chr7:5111200-5111600	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr7:5111200-5111800	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
19	chr7:5111200-5113600	ZNF genes & repeats	Spleen	Spleen
20	chr7:5111400-5111600	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
21	chr7:5111400-5111600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
22	chr7:5111400-5111600	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
23	chr7:5111400-5111600	Bivalent Enhancer	Primary T helper cells PMA-I stimulated	--
24	chr7:5111400-5111600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
25	chr7:5111400-5111600	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr7:5111400-5111600	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:5111400-5111600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr7:5111400-5111600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:5111400-5111600	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr7:5111400-5111600	Active TSS	Brain Anterior Caudate	brain
31	chr7:5111400-5111600	Enhancers	Brain Hippocampus Middle	brain
32	chr7:5111400-5111600	Bivalent Enhancer	Brain Dorsolateral Prefrontal Cortex	brain
33	chr7:5111400-5111600	Enhancers	Right Atrium	heart
34	chr7:5111400-5111600	Enhancers	Right Ventricle	heart
35	chr7:5111400-5111600	Flanking Active TSS	K562	blood
36	chr7:5111400-5111600	Enhancers	NHDF-Ad	bronchial
37	chr7:5111400-5111800	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
38	chr7:5111400-5111800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
39	chr7:5111400-5111800	Bivalent Enhancer	Brain Germinal Matrix	brain
40	chr7:5111400-5111800	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
41	chr7:5111400-5111800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr7:5111400-5111800	Enhancers	Left Ventricle	heart
43	chr7:5111400-5112000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr7:5111400-5112000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:5111400-5112000	Flanking Bivalent TSS/Enh	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr7:5111400-5112000	ZNF genes & repeats	Adipose Nuclei	Adipose
47	chr7:5111400-5112000	Bivalent Enhancer	Placenta	Placenta
48	chr7:5111400-5112000	ZNF genes & repeats	Lung	lung
49	chr7:5111400-5112000	Enhancers	Pancreas	Pancrea
50	chr7:5111400-5112200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood

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