Variant report

Variant	esv3331508
Chromosome Location	chr7:6460277-6462225
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:24)
CpG islands
(count:183)
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	CBX3	chr7:6461097-6461508	K562	blood:	n/a	n/a
2	POLR2A	chr7:6461232-6461384	GM12878	blood:	n/a	n/a
3	POLR2A	chr7:6461240-6461422	Hela-S3	cervix:	n/a	n/a
4	POLR2A	chr7:6460144-6460649	Hela-S3	cervix:	n/a	n/a
5	POLR2A	chr7:6461551-6461708	H1-hESC	embryonic stem cell:	n/a	n/a
6	POLR2A	chr7:6461237-6461550	H1-hESC	embryonic stem cell:	n/a	n/a
7	POLR2A	chr7:6461877-6461939	Hela-S3	cervix:	n/a	n/a
8	POLR2A	chr7:6460091-6460887	HL-60	blood:	n/a	n/a
9	POLR2A	chr7:6461337-6461540	HUVEC	blood vessel:	n/a	n/a
10	POLR2A	chr7:6460274-6460704	A549	lung:	n/a	n/a
11	POLR2A	chr7:6460205-6460293	K562	blood:	n/a	n/a
12	POLR2A	chr7:6461986-6462221	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr7:6460084-6460284	Hela-S3	cervix:	n/a	n/a
14	POLR2A	chr7:6462126-6462138	HepG2	liver:	n/a	n/a
15	POLR2A	chr7:6460045-6460734	SK-N-MC	brain:	n/a	n/a
16	POLR2A	chr7:6461384-6461490	HepG2	liver:	n/a	n/a
17	POLR2A	chr7:6461347-6461379	HepG2	liver:	n/a	n/a
18	POLR2A	chr7:6461216-6462754	SK-N-MC	brain:	n/a	n/a
19	POLR2A	chr7:6460197-6460403	U87	brain:	n/a	n/a
20	POLR2A	chr7:6461399-6462031	Hela-S3	cervix:	n/a	n/a
21	POLR2A	chr7:6460438-6460495	HepG2	liver:	n/a	n/a
22	POLR2A	chr7:6461226-6462504	HL-60	blood:	n/a	n/a
23	POLR2A	chr7:6461793-6461883	HUVEC	blood vessel:	n/a	n/a
24	TBL1XR1	chr7:6460610-6460636	K562	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:6461393-6461443	GM12878	blood:	n/a
2	chr7:6461991-6462041	HRPEpiC	eye:	n/a
3	chr7:6461393-6461443	HEEpiC	esophagus:	n/a
4	chr7:6461991-6462041	SKMC	muscle:	n/a
5	chr7:6461991-6462041	AG04450	lung:	fetal
6	chr7:6461991-6462041	SK-N-SH_RA	brain:	n/a
7	chr7:6460966-6461016	HL-60	blood:	n/a
8	chr7:6461991-6462041	SAEC	small airway:	n/a
9	chr7:6461991-6462041	A549	lung:	n/a
10	chr7:6460966-6461016	SK-N-MC	brain:	n/a
11	chr7:6460966-6461016	Hela-S3	cervix:	n/a
12	chr7:6461393-6461443	HL-60	blood:	n/a
13	chr7:6460966-6461016	MCF10A-Er-Src	breast:	n/a
14	chr7:6461393-6461443	NT2-D1	testis:	n/a
15	chr7:6460966-6461016	RPTEC	kidney:	n/a
16	chr7:6461393-6461443	HRE	kidney:	n/a
17	chr7:6461991-6462041	AG09319	gingival:	n/a
18	chr7:6460966-6461016	HPAEpiC	pulmonary alveolar:	n/a
19	chr7:6460966-6461016	SKMC	muscle:	n/a
20	chr7:6461991-6462041	H1-hESC	embryonic stem cell:	embryo
21	chr7:6461393-6461443	HAEpiC	amniotic membrane:	n/a
22	chr7:6461991-6462041	Caco-2	colon:	n/a
23	chr7:6460966-6461016	NT2-D1	testis:	n/a
24	chr7:6461991-6462041	HRE	kidney:	n/a
25	chr7:6461393-6461443	H1-hESC	embryonic stem cell:	embryo
26	chr7:6461991-6462041	SK-N-MC	brain:	n/a
27	chr7:6460966-6461016	HAEpiC	amniotic membrane:	n/a
28	chr7:6461393-6461443	AG10803	skin:	n/a
29	chr7:6461393-6461443	SK-N-SH_RA	brain:	n/a
30	chr7:6460966-6461016	HCF	heart:	n/a
31	chr7:6461393-6461443	A549	lung:	n/a
32	chr7:6460966-6461016	HEEpiC	esophagus:	n/a
33	chr7:6461991-6462041	AG04449	skin:	fetal
34	chr7:6461991-6462041	HCF	heart:	n/a
35	chr7:6461393-6461443	HRPEpiC	eye:	n/a
36	chr7:6461393-6461443	HCT-116	colon:	n/a
37	chr7:6460966-6461016	HUVEC	blood vessel:	n/a
38	chr7:6460966-6461016	Caco-2	colon:	n/a
39	chr7:6461991-6462041	IMR90	lung:	fetal
40	chr7:6461991-6462041	HMEC	breast:	n/a
41	chr7:6461991-6462041	MCF10A-Er-Src	breast:	n/a
42	chr7:6461393-6461443	Jurkat	blood:	n/a
43	chr7:6461991-6462041	SK-N-SH	brain:	n/a
44	chr7:6461393-6461443	HCPEpiC	choroid plexus:	n/a
45	chr7:6461393-6461443	NHDF-neo	bronchial:	n/a
46	chr7:6461991-6462041	GM12891	blood:	n/a
47	chr7:6460966-6461016	T-47D	breast:	n/a
48	chr7:6460966-6461016	Jurkat	blood:	n/a
49	chr7:6461991-6462041	LNCaP	prostate:	n/a
50	chr7:6460966-6461016	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr7:6459412..6462059-chr7:6463875..6466225,2	K562	blood:
2	chr7:6454958..6457155-chr7:6459947..6462538,2	MCF-7	breast:
3	chr7:6459143..6461711-chr7:6462987..6466871,3	K562	blood:

No data

Variant related genes	Relation type
DAGLB	TF binding region
DAGLB	CpG island
ENSG00000164535	chromatin interactions

Extended variants
information (count: 145 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:145 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529776652	chr7:6460281-6460282	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs548807120	chr7:6460284-6460285	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs115286533	chr7:6460298-6460299	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs141000277	chr7:6460301-6460302	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372750846	chr7:6460304-6460305	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559180561	chr7:6460305-6460306	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs116711919	chr7:6460308-6460309	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs186351782	chr7:6460309-6460310	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs538253892	chr7:6460313-6460314	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs117781377	chr7:6460320-6460321	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs574595098	chr7:6460329-6460330	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs541918315	chr7:6460335-6460336	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs72094559	chr7:6460359-6460360	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs367711257	chr7:6460361-6460362	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs201557901	chr7:6460365-6460366	Strong transcription Weak transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554384434	chr7:6460417-6460418	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs113981908	chr7:6460418-6460419	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs559628570	chr7:6460430-6460431	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112037091	chr7:6460493-6460494	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs572686835	chr7:6460494-6460495	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs540188090	chr7:6460532-6460533	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577204424	chr7:6460536-6460537	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs190649673	chr7:6460550-6460551	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs182892673	chr7:6460566-6460567	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562968202	chr7:6460578-6460579	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs73676739	chr7:6460583-6460584	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548289424	chr7:6460596-6460597	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567096828	chr7:6460624-6460625	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs549979927	chr7:6460637-6460638	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs375874591	chr7:6460664-6460665	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs10230345	chr7:6460671-6460672	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187798693	chr7:6460676-6460677	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs60038667	chr7:6460694-6460695	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs549074029	chr7:6460696-6460697	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs550195301	chr7:6460789-6460790	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs573521525	chr7:6460816-6460817	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568104423	chr7:6460845-6460846	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs112086111	chr7:6460846-6460847	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs150133878	chr7:6460847-6460848	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs66634073	chr7:6460867-6460868	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs577198792	chr7:6460899-6460900	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373536880	chr7:6460902-6460903	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs192908016	chr7:6460904-6460905	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs368231485	chr7:6460917-6460918	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs71808100	chr7:6460939-6460940	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201405283	chr7:6460940-6460941	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs199822139	chr7:6460943-6460944	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs563907604	chr7:6460945-6460946	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs199517914	chr7:6460951-6460952	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs558428631	chr7:6460962-6460963	Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:74)

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

Chromatin state (count:191 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:6426000-6475600	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:6437600-6470400	Strong transcription	Fetal Brain Female	brain
3	chr7:6438000-6462400	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr7:6438600-6475600	Strong transcription	HUES48 Cell Line	embryonic stem cell
5	chr7:6438800-6462800	Strong transcription	Primary T helper cells fromperipheralblood	blood
6	chr7:6439600-6472400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
7	chr7:6439800-6474600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr7:6439800-6474600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr7:6439800-6477400	Strong transcription	Fetal Intestine Small	intestine
10	chr7:6440200-6461400	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr7:6440200-6464600	Weak transcription	Right Atrium	heart
12	chr7:6440800-6460600	Strong transcription	Primary monocytes fromperipheralblood	blood
13	chr7:6441200-6471400	Strong transcription	Brain Germinal Matrix	brain
14	chr7:6443800-6465200	Weak transcription	Fetal Heart	heart
15	chr7:6443800-6475000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
16	chr7:6444000-6474600	Strong transcription	Lung	lung
17	chr7:6448600-6470000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
18	chr7:6450400-6460600	Weak transcription	Fetal Brain Male	brain
19	chr7:6450400-6475000	Strong transcription	Fetal Stomach	stomach
20	chr7:6452600-6461400	Weak transcription	K562	blood
21	chr7:6452800-6475000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr7:6453000-6463600	Weak transcription	GM12878-XiMat	blood
23	chr7:6453000-6486800	Weak transcription	Small Intestine	intestine
24	chr7:6453600-6483200	Weak transcription	Fetal Kidney	kidney
25	chr7:6454600-6463600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr7:6456600-6464400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr7:6456600-6475200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
28	chr7:6456800-6460400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr7:6456800-6460400	Weak transcription	Aorta	Aorta
30	chr7:6456800-6461200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr7:6456800-6461200	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr7:6456800-6464000	Weak transcription	Stomach Mucosa	stomach
33	chr7:6456800-6486800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr7:6457000-6464000	Weak transcription	Colon Smooth Muscle	Colon
35	chr7:6457200-6460400	Weak transcription	Primary T helper cells PMA-I stimulated	--
36	chr7:6457200-6460400	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr7:6457200-6461400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
38	chr7:6457200-6464000	Weak transcription	Primary B cells from cord blood	blood
39	chr7:6457400-6460400	Weak transcription	Left Ventricle	heart
40	chr7:6457400-6461600	Weak transcription	Brain Substantia Nigra	brain
41	chr7:6457400-6462800	Strong transcription	Placenta	Placenta
42	chr7:6457400-6463400	Weak transcription	HepG2	liver
43	chr7:6457400-6463600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr7:6457400-6464200	Weak transcription	Rectal Smooth Muscle	rectum
45	chr7:6457600-6461400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr7:6457800-6474800	Strong transcription	Thymus	Thymus
47	chr7:6458600-6460400	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chr7:6458800-6460400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr7:6458800-6460800	Genic enhancers	Fetal Muscle Trunk	muscle
50	chr7:6458800-6461600	Strong transcription	Primary neutrophils fromperipheralblood	blood

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