Variant report

Variant	esv3390705
Chromosome Location	chr7:5425826-5430724
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:48)
CpG islands
(count:427)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:48 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr7:5428102-5428108	K562	blood:	n/a	n/a
2	CCNT2	chr7:5427875-5427877	K562	blood:	n/a	n/a
3	CEBPB	chr7:5429206-5429215	HepG2	liver:	n/a	n/a
4	CTCF	chr7:5428311-5428362	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr7:5427607-5427700	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr7:5429180-5429330	GM12875	blood:	n/a	n/a
7	E2F6	chr7:5428445-5428768	H1-hESC	embryonic stem cell:	n/a	n/a
8	GABPA	chr7:5427270-5429069	H1-hESC	embryonic stem cell:	n/a	n/a
9	GABPA	chr7:5427177-5429069	H1-hESC	embryonic stem cell:	n/a	n/a
10	HMGN3	chr7:5427392-5427475	K562	blood:	n/a	n/a
11	MAX	chr7:5428364-5428840	H1-hESC	embryonic stem cell:	n/a	n/a
12	MAX	chr7:5428117-5428810	H1-hESC	embryonic stem cell:	n/a	n/a
13	POLR2A	chr7:5427895-5427944	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr7:5427646-5427705	HepG2	liver:	n/a	n/a
15	POLR2A	chr7:5429065-5429392	HepG2	liver:	n/a	n/a
16	POLR2A	chr7:5427355-5427448	A549	lung:	n/a	n/a
17	POLR2A	chr7:5425791-5426218	HepG2	liver:	n/a	n/a
18	POLR2A	chr7:5428452-5428558	A549	lung:	n/a	n/a
19	POLR2A	chr7:5426892-5427778	NB4	blood:	n/a	n/a
20	POLR2A	chr7:5426962-5426976	K562	blood:	n/a	n/a
21	POLR2A	chr7:5430015-5430470	HL-60	blood:	n/a	n/a
22	POLR2A	chr7:5429684-5429702	Hela-S3	cervix:	n/a	n/a
23	POLR2A	chr7:5427132-5427759	H1-neurons	neurons:	n/a	n/a
24	POLR2A	chr7:5429662-5429871	HepG2	liver:	n/a	n/a
25	POLR2A	chr7:5427189-5427848	PANC-1	pancreas:	n/a	n/a
26	POLR2A	chr7:5430024-5430904	PANC-1	pancreas:	n/a	n/a
27	POLR2A	chr7:5429573-5429651	Hela-S3	cervix:	n/a	n/a
28	POLR2A	chr7:5427544-5427601	Hela-S3	cervix:	n/a	n/a
29	POLR2A	chr7:5430595-5430754	HepG2	liver:	n/a	n/a
30	POLR2A	chr7:5430695-5430738	Hela-S3	cervix:	n/a	n/a
31	POLR2A	chr7:5428442-5428919	ECC-1	luminal epithelium:	n/a	n/a
32	POLR2A	chr7:5427282-5427480	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr7:5427772-5428102	GM12878	blood:	n/a	n/a
34	POLR2A	chr7:5430723-5430786	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr7:5426970-5427068	HepG2	liver:	n/a	n/a
36	POLR2A	chr7:5430057-5430938	PANC-1	pancreas:	n/a	n/a
37	POLR2A	chr7:5427850-5428054	HCT-116	colon:	n/a	n/a
38	POLR2A	chr7:5428930-5429044	A549	lung:	n/a	n/a
39	POLR2A	chr7:5428729-5428840	ProgFib	skin:	n/a	n/a
40	POLR2A	chr7:5426779-5427035	ECC-1	luminal epithelium:	n/a	n/a
41	POLR2A	chr7:5427139-5427969	HL-60	blood:	n/a	n/a
42	POLR2A	chr7:5430506-5430974	HL-60	blood:	n/a	n/a
43	RAD21	chr7:5427203-5427425	H1-hESC	embryonic stem cell:	n/a	n/a
44	RAD21	chr7:5428184-5428672	H1-hESC	embryonic stem cell:	n/a	n/a
45	RAD21	chr7:5427257-5427413	H1-hESC	embryonic stem cell:	n/a	n/a
46	RAD21	chr7:5427215-5427597	H1-hESC	embryonic stem cell:	n/a	n/a
47	ZKSCAN1	chr7:5426768-5426985	Hela-S3	cervix:	n/a	n/a
48	ZNF143	chr7:5430638-5430789	H1-hESC	embryonic stem cell:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:5427647-5427697	NB4	blood:	n/a
2	chr7:5427244-5427294	AG04449	skin:	fetal
3	chr7:5428633-5428683	SK-N-SH	brain:	n/a
4	chr7:5426831-5426881	HEEpiC	esophagus:	n/a
5	chr7:5428633-5428683	PANC-1	pancreas:	n/a
6	chr7:5429036-5429086	HRE	kidney:	n/a
7	chr7:5427647-5427697	H1-hESC	embryonic stem cell:	embryo
8	chr7:5426831-5426881	CMK	blood:	n/a
9	chr7:5429036-5429086	GM06990	blood:	n/a
10	chr7:5426831-5426881	NT2-D1	testis:	n/a
11	chr7:5429036-5429086	A549	lung:	n/a
12	chr7:5429036-5429086	HCM	heart:	n/a
13	chr7:5429036-5429086	HCT-116	colon:	n/a
14	chr7:5427647-5427697	HEEpiC	esophagus:	n/a
15	chr7:5427244-5427294	HPAEpiC	pulmonary alveolar:	n/a
16	chr7:5427647-5427697	AoSMC	blood vessel:	n/a
17	chr7:5429428-5429478	SAEC	small airway:	n/a
18	chr7:5427647-5427697	AG04449	skin:	fetal
19	chr7:5429036-5429086	K562	blood:	n/a
20	chr7:5426831-5426881	GM12892	blood:	n/a
21	chr7:5427244-5427294	HL-60	blood:	n/a
22	chr7:5427647-5427697	GM19239	blood:	n/a
23	chr7:5429428-5429478	SK-N-SH	brain:	n/a
24	chr7:5428633-5428683	Hela-S3	cervix:	n/a
25	chr7:5429036-5429086	HAEpiC	amniotic membrane:	n/a
26	chr7:5429428-5429478	GM06990	blood:	n/a
27	chr7:5427244-5427294	SK-N-MC	brain:	n/a
28	chr7:5426831-5426881	U87	brain:	n/a
29	chr7:5428633-5428683	Hepatocyte	liver:	n/a
30	chr7:5426831-5426881	HMEC	breast:	n/a
31	chr7:5429036-5429086	NHDF-neo	bronchial:	n/a
32	chr7:5429036-5429086	AG04450	lung:	fetal
33	chr7:5427647-5427697	BJ	skin:	n/a
34	chr7:5427244-5427294	NB4	blood:	n/a
35	chr7:5429428-5429478	NB4	blood:	n/a
36	chr7:5428633-5428683	BJ	skin:	n/a
37	chr7:5426831-5426881	HCF	heart:	n/a
38	chr7:5428633-5428683	HCT-116	colon:	n/a
39	chr7:5429428-5429478	T-47D	breast:	n/a
40	chr7:5426831-5426881	SK-N-MC	brain:	n/a
41	chr7:5428633-5428683	GM12891	blood:	n/a
42	chr7:5429428-5429478	NH-A	brain:	n/a
43	chr7:5429036-5429086	GM12878	blood:	n/a
44	chr7:5426831-5426881	T-47D	breast:	n/a
45	chr7:5429428-5429478	HCM	heart:	n/a
46	chr7:5429036-5429086	T-47D	breast:	n/a
47	chr7:5427647-5427697	PFSK-1	brain:	n/a
48	chr7:5427647-5427697	HPAEpiC	pulmonary alveolar:	n/a
49	chr7:5428633-5428683	SK-N-MC	brain:	n/a
50	chr7:5428014-5428064	GM19239	blood:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:5420732..5423186-chr7:5425259..5427446,2	MCF-7	breast:
2	chr7:5426046..5429721-chr7:5429735..5433041,4	K562	blood:
3	chr7:5428152..5429787-chr7:5466437..5469145,2	K562	blood:
4	chr7:5420460..5423379-chr7:5428515..5430331,2	MCF-7	breast:
5	chr7:5424305..5426249-chr7:5463698..5466479,2	MCF-7	breast:
6	chr7:5406257..5408361-chr7:5427751..5430730,2	MCF-7	breast:
7	chr7:5427419..5438627-chr7:5461902..5471481,26	MCF-7	breast:
8	chr7:5429619..5431536-chr7:5464762..5466326,2	K562	blood:

No data

Variant related genes	Relation type
TNRC18	TF binding region
TNRC18	CpG island
ENSG00000273084	chromatin interactions
ENSG00000272953	chromatin interactions
ENSG00000182095	chromatin interactions
ENSG00000234432	chromatin interactions

Extended variants
information (count: 244 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:244 , 50 per page) page: 1 2 3 4 5

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs551473003	chr7:5425833-5425834	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs569745954	chr7:5425858-5425859	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs537177400	chr7:5425895-5425896	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs200976474	chr7:5425906-5425907	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs28767812	chr7:5425945-5425946	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs534869597	chr7:5425951-5425952	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs552999250	chr7:5425984-5425985	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs189426726	chr7:5425989-5425990	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs544785239	chr7:5426016-5426017	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs139937733	chr7:5426065-5426066	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs575328188	chr7:5426087-5426088	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs560449687	chr7:5426138-5426139	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs181704477	chr7:5426191-5426192	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs56339818	chr7:5426198-5426199	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs370435749	chr7:5426205-5426206	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs202182277	chr7:5426213-5426214	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs57427019	chr7:5426218-5426219	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs543196469	chr7:5426237-5426238	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs528487862	chr7:5426239-5426240	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs145469203	chr7:5426249-5426250	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs561820538	chr7:5426281-5426282	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565599586	chr7:5426323-5426324	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs532883202	chr7:5426339-5426340	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28689492	chr7:5426360-5426361	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs140487386	chr7:5426399-5426400	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs528951463	chr7:5426412-5426413	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs530616370	chr7:5426427-5426428	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs371933161	chr7:5426443-5426444	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs58213418	chr7:5426481-5426482	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs567211163	chr7:5426563-5426564	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs534345936	chr7:5426613-5426614	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552963357	chr7:5426624-5426625	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560969710	chr7:5426635-5426636	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs12666408	chr7:5426637-5426638	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538591457	chr7:5426646-5426647	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556735347	chr7:5426656-5426657	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369280209	chr7:5426671-5426672	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs148903510	chr7:5426672-5426673	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs559358840	chr7:5426678-5426679	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs372441340	chr7:5426684-5426685	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs143423784	chr7:5426688-5426689	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs111779220	chr7:5426695-5426696	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186883774	chr7:5426701-5426702	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs540241402	chr7:5426706-5426707	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs565312319	chr7:5426763-5426764	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551632060	chr7:5426793-5426794	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs532845592	chr7:5426831-5426832	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs74496206	chr7:5426837-5426838	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs191473020	chr7:5426863-5426864	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs530238194	chr7:5426881-5426882	Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Bladder cancer	21909424	CNVD
Glioblastoma multiforme	21525872	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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:320 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:5410200-5426800	Weak transcription	HUVEC	blood vessel
2	chr7:5410200-5429200	Weak transcription	Primary B cells from cord blood	blood
3	chr7:5413600-5426800	Weak transcription	HSMMtube	muscle
4	chr7:5413600-5435000	Weak transcription	HSMM	muscle
5	chr7:5413800-5426800	Weak transcription	HMEC	breast
6	chr7:5416800-5430400	Weak transcription	GM12878-XiMat	blood
7	chr7:5417600-5426200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr7:5422000-5426800	Weak transcription	K562	blood
9	chr7:5422400-5426800	Weak transcription	Pancreatic Islets	Pancreatic Islet
10	chr7:5422600-5426800	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr7:5422600-5426800	Weak transcription	Fetal Kidney	kidney
12	chr7:5422600-5431800	Strong transcription	Primary neutrophils fromperipheralblood	blood
13	chr7:5423000-5426800	Weak transcription	NH-A	brain
14	chr7:5423000-5431600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr7:5423000-5434000	Strong transcription	Fetal Thymus	thymus
16	chr7:5423200-5426800	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr7:5423200-5426800	Weak transcription	Brain Cingulate Gyrus	brain
18	chr7:5423200-5426800	Weak transcription	NHDF-Ad	bronchial
19	chr7:5423200-5427400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
20	chr7:5423200-5428200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr7:5423200-5435200	Strong transcription	Fetal Intestine Large	intestine
22	chr7:5423200-5436400	Weak transcription	Right Atrium	heart
23	chr7:5423400-5426200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr7:5423400-5426600	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr7:5423400-5426800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
26	chr7:5423400-5426800	Weak transcription	Brain Substantia Nigra	brain
27	chr7:5423400-5436400	Strong transcription	Fetal Intestine Small	intestine
28	chr7:5423400-5436400	Weak transcription	Psoas Muscle	Psoas
29	chr7:5423600-5426800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr7:5423600-5426800	Weak transcription	Fetal Lung	lung
31	chr7:5423600-5434800	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:5423600-5443600	Weak transcription	Fetal Brain Male	brain
33	chr7:5424000-5434200	Strong transcription	Thymus	Thymus
34	chr7:5424000-5437600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr7:5424200-5428200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr7:5424400-5426800	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr7:5424400-5426800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr7:5424400-5426800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
39	chr7:5424400-5428000	Strong transcription	Duodenum Mucosa	Duodenum
40	chr7:5424400-5439200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr7:5424600-5426200	Weak transcription	Brain Germinal Matrix	brain
42	chr7:5424600-5426400	Weak transcription	Brain Anterior Caudate	brain
43	chr7:5424600-5426600	Weak transcription	Hela-S3	cervix
44	chr7:5424600-5426800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr7:5424600-5426800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr7:5424600-5426800	Weak transcription	HepG2	liver
47	chr7:5424600-5426800	Weak transcription	NHEK	skin
48	chr7:5424600-5427400	Strong transcription	Primary B cells from peripheral blood	blood
49	chr7:5424600-5428000	Strong transcription	Primary monocytes fromperipheralblood	blood
50	chr7:5424600-5434200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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