Variant report

Variant	esv3360264
Chromosome Location	chr7:6691327-6695325
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:81)
CpG islands
(count:672)
Chromatin interactive
region (count:6)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:81 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr7:6693271-6693492	GM12878	blood:	n/a	n/a
2	BCL3	chr7:6693791-6694049	GM12878	blood:	n/a	n/a
3	CCNT2	chr7:6694042-6694139	K562	blood:	n/a	n/a
4	ELF1	chr7:6694512-6694819	GM12878	blood:	n/a	n/a
5	ELF1	chr7:6693518-6693985	GM12878	blood:	n/a	n/a
6	GABPA	chr7:6693265-6693772	H1-hESC	embryonic stem cell:	n/a	n/a
7	GABPA	chr7:6693871-6694198	H1-hESC	embryonic stem cell:	n/a	n/a
8	HMGN3	chr7:6692437-6692466	K562	blood:	n/a	n/a
9	MYC	chr7:6693497-6693638	MCF-7	breast:	n/a	n/a
10	MYC	chr7:6692304-6692375	MCF-7	breast:	n/a	n/a
11	PAX5	chr7:6692302-6692682	GM12878	blood:	n/a	n/a
12	PAX5	chr7:6693717-6694116	GM12891	blood:	n/a	chr7:6693933-6693952
13	PAX5	chr7:6693740-6694153	GM12878	blood:	n/a	chr7:6693933-6693952
14	PAX5	chr7:6693471-6694164	GM12892	blood:	n/a	chr7:6693933-6693952
15	PAX5	chr7:6693823-6694038	GM12892	blood:	n/a	chr7:6693933-6693952
16	PAX5	chr7:6692399-6692566	GM12878	blood:	n/a	n/a
17	PAX5	chr7:6693543-6694257	GM12878	blood:	n/a	chr7:6693933-6693952
18	PAX5	chr7:6692292-6692760	GM12878	blood:	n/a	n/a
19	PAX5	chr7:6693715-6694061	GM12878	blood:	n/a	chr7:6693933-6693952
20	PAX5	chr7:6692203-6692749	GM12878	blood:	n/a	n/a
21	PAX5	chr7:6692099-6692801	GM12892	blood:	n/a	n/a
22	PAX5	chr7:6692282-6692683	GM12891	blood:	n/a	n/a
23	PBX3	chr7:6693289-6693652	GM12878	blood:	n/a	n/a
24	PBX3	chr7:6693877-6694030	GM12878	blood:	n/a	n/a
25	POLR2A	chr7:6693703-6693707	MCF-7	breast:	n/a	n/a
26	POLR2A	chr7:6692113-6692728	GM12892	blood:	n/a	n/a
27	POLR2A	chr7:6692197-6692397	K562	blood:	n/a	n/a
28	POLR2A	chr7:6694257-6694677	GM12878	blood:	n/a	n/a
29	POLR2A	chr7:6694042-6694952	GM12878	blood:	n/a	n/a
30	POLR2A	chr7:6693262-6693986	GM12878	blood:	n/a	n/a
31	POLR2A	chr7:6693825-6693969	MCF-7	breast:	n/a	n/a
32	POLR2A	chr7:6694059-6696588	K562	blood:	n/a	n/a
33	POLR2A	chr7:6695012-6695052	K562	blood:	n/a	n/a
34	POLR2A	chr7:6691834-6692147	K562	blood:	n/a	n/a
35	POLR2A	chr7:6693515-6693701	MCF-7	breast:	n/a	n/a
36	POLR2A	chr7:6694999-6696158	GM12892	blood:	n/a	n/a
37	POLR2A	chr7:6692514-6692526	MCF-7	breast:	n/a	n/a
38	POLR2A	chr7:6695265-6695399	HepG2	liver:	n/a	n/a
39	POLR2A	chr7:6693871-6693922	K562	blood:	n/a	n/a
40	POLR2A	chr7:6693210-6694064	GM12878	blood:	n/a	n/a
41	POLR2A	chr7:6691342-6691618	K562	blood:	n/a	n/a
42	POLR2A	chr7:6695304-6695471	K562	blood:	n/a	n/a
43	POLR2A	chr7:6692822-6693107	GM12878	blood:	n/a	n/a
44	POLR2A	chr7:6694329-6694770	GM12892	blood:	n/a	n/a
45	POLR2A	chr7:6693197-6693474	K562	blood:	n/a	n/a
46	POLR2A	chr7:6694457-6694719	K562	blood:	n/a	n/a
47	POLR2A	chr7:6695246-6696805	K562	blood:	n/a	n/a
48	POLR2A	chr7:6692020-6692692	GM12878	blood:	n/a	n/a
49	POLR2A	chr7:6693936-6693957	K562	blood:	n/a	n/a
50	POLR2A	chr7:6695160-6695987	GM12892	blood:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6694373-6694423	HMEC	breast:	n/a
2	chr7:6694373-6694423	HMEC	breast:	n/a
3	chr7:6693838-6693888	NHDF-neo	bronchial:	n/a
4	chr7:6692445-6692495	PrEC	prostate:	n/a
5	chr7:6692873-6692923	LNCaP	prostate:	n/a
6	chr7:6694978-6695028	AG04449	skin:	fetal
7	chr7:6694735-6694785	NT2-D1	testis:	n/a
8	chr7:6693838-6693888	PrEC	prostate:	n/a
9	chr7:6692873-6692923	MCF-7	breast:	n/a
10	chr7:6692445-6692495	HepG2	liver:	n/a
11	chr7:6695121-6695171	IMR90	lung:	fetal
12	chr7:6693838-6693888	NB4	blood:	n/a
13	chr7:6694978-6695028	NT2-D1	testis:	n/a
14	chr7:6695121-6695171	BE2_C	brain:	n/a
15	chr7:6693030-6693080	PANC-1	pancreas:	n/a
16	chr7:6692873-6692923	HCM	heart:	n/a
17	chr7:6694735-6694785	HCF	heart:	n/a
18	chr7:6694978-6695028	AG09309	skin:	n/a
19	chr7:6695092-6695142	LNCaP	prostate:	n/a
20	chr7:6691949-6691999	HRE	kidney:	n/a
21	chr7:6693334-6693384	SKMC	muscle:	n/a
22	chr7:6693030-6693080	HRE	kidney:	n/a
23	chr7:6691949-6691999	IMR90	lung:	fetal
24	chr7:6692445-6692495	GM06990	blood:	n/a
25	chr7:6691949-6691999	PFSK-1	brain:	n/a
26	chr7:6692445-6692495	ProgFib	skin:	n/a
27	chr7:6693838-6693888	AoSMC	blood vessel:	n/a
28	chr7:6693030-6693080	HAEpiC	amniotic membrane:	n/a
29	chr7:6692445-6692495	NHDF-neo	bronchial:	n/a
30	chr7:6691949-6691999	NHDF-neo	bronchial:	n/a
31	chr7:6691949-6691999	U87	brain:	n/a
32	chr7:6692445-6692495	Jurkat	blood:	n/a
33	chr7:6695121-6695171	GM12878	blood:	n/a
34	chr7:6691949-6691999	LNCaP	prostate:	n/a
35	chr7:6693838-6693888	MCF10A-Er-Src	breast:	n/a
36	chr7:6694373-6694423	U87	brain:	n/a
37	chr7:6693334-6693384	HepG2	liver:	n/a
38	chr7:6693030-6693080	SK-N-MC	brain:	n/a
39	chr7:6691949-6691999	HCPEpiC	choroid plexus:	n/a
40	chr7:6694373-6694423	NHDF-neo	bronchial:	n/a
41	chr7:6692445-6692495	AG09309	skin:	n/a
42	chr7:6692445-6692495	HPAEpiC	pulmonary alveolar:	n/a
43	chr7:6692445-6692495	AG10803	skin:	n/a
44	chr7:6695092-6695142	AG04449	skin:	fetal
45	chr7:6694373-6694423	GM19239	blood:	n/a
46	chr7:6694978-6695028	U87	brain:	n/a
47	chr7:6694978-6695028	BJ	skin:	n/a
48	chr7:6693334-6693384	IMR90	lung:	fetal
49	chr7:6693838-6693888	HCF	heart:	n/a
50	chr7:6691949-6691999	GM19239	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:6676518..6678447-chr7:6694438..6696514,2	MCF-7	breast:
2	chr7:6679487..6682483-chr7:6695124..6696654,2	MCF-7	breast:
3	chr7:6674759..6677679-chr7:6692100..6694240,3	MCF-7	breast:
4	chr7:6680998..6682837-chr7:6692889..6695214,2	MCF-7	breast:
5	chr7:6689485..6692014-chr7:6722455..6725146,3	MCF-7	breast:
6	chr7:6694849..6698438-chr7:6699530..6702045,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC073343.1-2	chr7:6694495-6696063	ENSG00000260054.1

No data

Variant related genes	Relation type
ENSG00000260054	TF binding region
ENSG00000260054	CpG island
ENSG00000205903	chromatin interactions

Extended variants
information (count: 135 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:135 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533920711	chr7:6691363-6691364	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs558957982	chr7:6691399-6691400	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs550286429	chr7:6691434-6691435	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs185659227	chr7:6691444-6691445	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs545331691	chr7:6691478-6691479	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs557148876	chr7:6691524-6691525	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs372483686	chr7:6691555-6691556	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs542712491	chr7:6691573-6691574	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs569891457	chr7:6691667-6691668	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs376574763	chr7:6691681-6691682	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs189510906	chr7:6691741-6691742	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs539842843	chr7:6691797-6691798	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs180763767	chr7:6691807-6691808	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs185212267	chr7:6691808-6691809	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs375872349	chr7:6691820-6691821	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs550865489	chr7:6691821-6691822	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs569081526	chr7:6691843-6691844	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs530245249	chr7:6691876-6691877	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs28613348	chr7:6691957-6691958	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs377196265	chr7:6691968-6691969	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
21	rs117515622	chr7:6691974-6691975	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
22	rs148609364	chr7:6691986-6691987	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
23	rs558639787	chr7:6692082-6692083	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs62439671	chr7:6692096-6692097	Weak transcription Strong transcription ZNF genes & repeats	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs3735302	chr7:6692105-6692106	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs189975373	chr7:6692137-6692138	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs575646947	chr7:6692142-6692143	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs542820737	chr7:6692151-6692152	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs554793791	chr7:6692203-6692204	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs572839621	chr7:6692227-6692228	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs369484052	chr7:6692229-6692230	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs373742099	chr7:6692247-6692248	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs564679858	chr7:6692261-6692262	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs576451588	chr7:6692277-6692278	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs376495708	chr7:6692291-6692292	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs562825244	chr7:6692353-6692354	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs530373612	chr7:6692367-6692368	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs548489831	chr7:6692379-6692380	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs560747381	chr7:6692432-6692433	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs527738311	chr7:6692441-6692442	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs142128577	chr7:6692445-6692446	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs570828662	chr7:6692453-6692454	Weak transcription Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs538228318	chr7:6692520-6692521	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs550230193	chr7:6692539-6692540	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs372507837	chr7:6692586-6692587	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs1474419	chr7:6692605-6692606	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs536588168	chr7:6692607-6692608	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs111969111	chr7:6692677-6692678	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs554424733	chr7:6692762-6692763	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs572995417	chr7:6692784-6692785	Weak transcription Strong transcription ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	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
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
Acute myeloid leukemia	21251322	CNVD
Glioblastoma multiforme	21525872	CNVD
Autism	20685689	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6678000-6691600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr7:6678200-6698200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:6678400-6691600	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr7:6678400-6691600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr7:6678800-6691400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr7:6679000-6692200	Strong transcription	Primary T cells from cord blood	blood
7	chr7:6679000-6692600	Strong transcription	Primary B cells from peripheral blood	blood
8	chr7:6679000-6695200	Strong transcription	Stomach Smooth Muscle	stomach
9	chr7:6679000-6695400	Strong transcription	Brain Inferior Temporal Lobe	brain
10	chr7:6679200-6695400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
11	chr7:6679400-6691600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
12	chr7:6679400-6691600	Strong transcription	Liver	Liver
13	chr7:6679400-6696400	Strong transcription	Brain Hippocampus Middle	brain
14	chr7:6679400-6703600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr7:6679600-6693200	Strong transcription	Rectal Smooth Muscle	rectum
16	chr7:6679600-6699200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
17	chr7:6679800-6695600	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr7:6680000-6691600	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
19	chr7:6680000-6692600	Strong transcription	Primary T helper cells PMA-I stimulated	--
20	chr7:6680000-6692600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr7:6680000-6695200	Strong transcription	Duodenum Mucosa	Duodenum
22	chr7:6680200-6691600	Strong transcription	Colonic Mucosa	Colon
23	chr7:6680200-6691800	Weak transcription	Fetal Brain Male	brain
24	chr7:6680400-6691600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr7:6680400-6691800	Strong transcription	Adipose Nuclei	Adipose
26	chr7:6680400-6691800	Strong transcription	Ovary	ovary
27	chr7:6680400-6694600	Strong transcription	Brain Cingulate Gyrus	brain
28	chr7:6680400-6695200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr7:6680400-6695600	Strong transcription	Rectal Mucosa Donor 29	rectum
30	chr7:6680400-6698600	Weak transcription	Right Atrium	heart
31	chr7:6680600-6691800	Strong transcription	Gastric	stomach
32	chr7:6680600-6692600	Strong transcription	Primary T cells fromperipheralblood	blood
33	chr7:6680600-6695200	Strong transcription	Duodenum Smooth Muscle	Duodenum
34	chr7:6680600-6695400	Strong transcription	Brain Anterior Caudate	brain
35	chr7:6680800-6692400	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr7:6681000-6693400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr7:6682400-6698800	Weak transcription	Fetal Kidney	kidney
38	chr7:6683200-6693400	Weak transcription	Stomach Mucosa	stomach
39	chr7:6683800-6696600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
40	chr7:6684000-6691800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
41	chr7:6684600-6691400	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr7:6684600-6694000	Weak transcription	NHDF-Ad	bronchial
43	chr7:6684600-6698200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr7:6684800-6691600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr7:6684800-6691600	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr7:6684800-6691800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chr7:6684800-6691800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr7:6684800-6691800	Weak transcription	Psoas Muscle	Psoas
49	chr7:6684800-6699000	Weak transcription	H9 Cell Line	embryonic stem cell
50	chr7:6685000-6691400	Weak transcription	Small Intestine	intestine

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