Variant report

Variant	esv2762654
Chromosome Location	chr7:16968409-16978915
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr7:16975016-16975338	Hela-S3	cervix:	n/a	n/a
2	CTCF	chr7:16974420-16974570	AG04449	skin:	n/a	n/a
3	CTCF	chr7:16974520-16974551	Fibrobl	skin:	n/a	n/a
4	CTCF	chr7:16970766-16970831	Kidney_OC	kidney:	n/a	n/a
5	CTCF	chr7:16978900-16979050	Caco-2	colon:	n/a	n/a
6	EBF1	chr7:16968871-16969116	GM12878	blood:	n/a	n/a
7	EBF1	chr7:16968812-16969153	GM12878	blood:	n/a	n/a
8	EBF1	chr7:16973569-16973781	GM12878	blood:	n/a	n/a
9	ELK1	chr7:16974596-16974629	Hela-S3	cervix:	n/a	n/a
10	EP300	chr7:16974982-16975377	Hela-S3	cervix:	n/a	n/a
11	EP300	chr7:16974959-16975406	T-47D	breast:	n/a	n/a
12	EP300	chr7:16974996-16975451	T-47D	breast:	n/a	n/a
13	FOS	chr7:16974687-16975335	MCF10A-Er-Src	breast:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
14	FOS	chr7:16978813-16979114	MCF10A-Er-Src	breast:	n/a	chr7:16978958-16978967
15	FOS	chr7:16974673-16975284	MCF10A-Er-Src	breast:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
16	FOS	chr7:16978811-16979085	MCF10A-Er-Src	breast:	n/a	chr7:16978958-16978967
17	FOS	chr7:16974557-16975385	HUVEC	blood vessel:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
18	FOS	chr7:16978809-16979131	MCF10A-Er-Src	breast:	n/a	chr7:16978958-16978967
19	FOS	chr7:16974633-16975263	MCF10A-Er-Src	breast:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
20	FOS	chr7:16978826-16979109	MCF10A-Er-Src	breast:	n/a	chr7:16978958-16978967
21	FOS	chr7:16974997-16975391	MCF10A-Er-Src	breast:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
22	FOSL1	chr7:16978695-16979235	HCT-116	colon:	n/a	chr7:16978958-16978967
23	FOSL1	chr7:16978723-16979100	HCT-116	colon:	n/a	chr7:16978958-16978967
24	FOSL1	chr7:16974480-16975318	HCT-116	colon:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
25	FOXA1	chr7:16973913-16974240	T-47D	breast:	n/a	n/a
26	FOXA1	chr7:16975096-16975517	T-47D	breast:	n/a	n/a
27	FOXA1	chr7:16974989-16975347	T-47D	breast:	n/a	n/a
28	FOXA1	chr7:16973906-16974313	T-47D	breast:	n/a	n/a
29	FOXA1	chr7:16975904-16976283	T-47D	breast:	n/a	n/a
30	GATA2	chr7:16974437-16975458	HUVEC	blood vessel:	n/a	chr7:16975446-16975456
31	GATA3	chr7:16974902-16975405	T-47D	breast:	n/a	n/a
32	GATA3	chr7:16974947-16975422	T-47D	breast:	n/a	n/a
33	GATA3	chr7:16974603-16975494	MCF-7	breast:	n/a	chr7:16975446-16975456
34	GATA3	chr7:16974968-16975503	MCF-7	breast:	n/a	chr7:16975446-16975456
35	GATA3	chr7:16973920-16974269	T-47D	breast:	n/a	n/a
36	GATA3	chr7:16973879-16974312	T-47D	breast:	n/a	n/a
37	JUND	chr7:16974978-16975519	T-47D	breast:	n/a	chr7:16975089-16975098 chr7:16975037-16975045
38	JUND	chr7:16978805-16979106	HCT-116	colon:	n/a	chr7:16978958-16978967
39	JUND	chr7:16978845-16979131	H1-hESC	embryonic stem cell:	n/a	chr7:16978958-16978967
40	MAFF	chr7:16976722-16976904	K562	blood:	n/a	chr7:16976837-16976855
41	MAFF	chr7:16976695-16977010	HepG2	liver:	n/a	chr7:16976837-16976855
42	MAFK	chr7:16976668-16976996	IMR90	lung:	n/a	chr7:16976838-16976853
43	MAFK	chr7:16976685-16977023	HepG2	liver:	n/a	chr7:16976838-16976853
44	MAFK	chr7:16976674-16977016	HepG2	liver:	n/a	chr7:16976838-16976853
45	MAFK	chr7:16976693-16976936	Hela-S3	cervix:	n/a	chr7:16976838-16976853
46	MAX	chr7:16968527-16968590	NB4	blood:	n/a	n/a
47	MAX	chr7:16969545-16969796	NB4	blood:	n/a	chr7:16969682-16969692
48	MYC	chr7:16975028-16975198	MCF10A-Er-Src	breast:	n/a	chr7:16975125-16975134
49	MYC	chr7:16975005-16975218	MCF10A-Er-Src	breast:	n/a	chr7:16975125-16975134
50	NR2F2	chr7:16975054-16975459	MCF-7	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr7:16968832..16971770-chr7:16973554..16975101,2	MCF-7	breast:
2	chr7:16973110..16976162-chr7:16977705..16980003,3	K562	blood:
3	chr7:16966075..16967859-chr7:16969900..16971992,2	MCF-7	breast:
4	chr11:83411053..83411898-chr7:16967815..16968540,2	MCF-7	breast:
5	chr7:16960280..16962673-chr7:16969030..16970953,2	MCF-7	breast:
6	chr7:16966017..16967722-chr7:16978514..16980998,2	MCF-7	breast:
7	chr7:16973521..16976963-chr7:16980270..16983523,4	MCF-7	breast:
8	chr7:16968832..16971770-chr7:16973554..16975101,2	MCF-7	breast:
9	chr7:16973925..16976162-chr7:16977721..16980003,2	K562	blood:
10	chr7:16974533..16976554-chr7:17579096..17580960,2	K562	blood:
11	chr7:16973446..16975003-chr7:17029206..17031058,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN13-2	chr7:16977849-16978181	NONHSAT119309

Variant related genes	Relation type
ENSG00000223867	TF binding region
ENSG00000223867	chromatin interactions

Extended variants
information (count: 444 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4333473	chr7:16968409-16968410	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs847397	chr7:16968457-16968458	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs114216959	chr7:16968467-16968468	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114874966	chr7:16968468-16968469	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144426062	chr7:16968474-16968475	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs183737089	chr7:16968508-16968509	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs847396	chr7:16968509-16968510	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs188284410	chr7:16968528-16968529	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538451843	chr7:16968564-16968565	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs10228868	chr7:16968585-16968586	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs533290743	chr7:16968593-16968594	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs375651061	chr7:16968616-16968617	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs578201472	chr7:16968650-16968651	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545063488	chr7:16968658-16968659	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560516413	chr7:16968671-16968672	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs369547265	chr7:16968756-16968757	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs543177476	chr7:16968766-16968767	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs10258836	chr7:16968767-16968768	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs192618231	chr7:16968771-16968772	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs118126807	chr7:16968779-16968780	Weak transcription ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs137943338	chr7:16968822-16968823	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs367767644	chr7:16968892-16968893	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs533300321	chr7:16968899-16968900	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs75475696	chr7:16968904-16968905	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs371328293	chr7:16968905-16968906	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs566161235	chr7:16968938-16968939	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs142439939	chr7:16968974-16968975	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs548636609	chr7:16968988-16968989	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs567379279	chr7:16968989-16968990	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs538011755	chr7:16969004-16969005	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs375622341	chr7:16969006-16969007	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs556754514	chr7:16969018-16969019	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs368595786	chr7:16969022-16969023	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs372059018	chr7:16969027-16969028	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs11982559	chr7:16969043-16969044	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs572434603	chr7:16969054-16969055	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs201862943	chr7:16969061-16969062	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs540815066	chr7:16969091-16969092	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs146008583	chr7:16969095-16969096	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs561195450	chr7:16969157-16969158	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs555073066	chr7:16969169-16969170	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs576497148	chr7:16969192-16969193	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs544060983	chr7:16969202-16969203	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs562730844	chr7:16969212-16969213	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs201366790	chr7:16969233-16969234	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs139916612	chr7:16969252-16969253	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs369435222	chr7:16969257-16969258	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs185355760	chr7:16969260-16969261	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs190129495	chr7:16969344-16969345	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs527237843	chr7:16969358-16969359	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Melanoma	18172304	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
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21364760	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Leukemia	23979775	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Autism	22495311	CNVD
Prostate cancer	16573809	CNVD
Acute myeloid leukemia	21251322	CNVD
Melanoma	17363583	CNVD
Kartagener syndrome	16639409	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Prostate cancer	19242612	CNVD
Autism	18414403	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	21858162	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Cancer	21637783	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Glioblastoma multiforme	18628472	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Rubinstein-Taybi syndrome	22470819	CNVD
Alzheimer''s disease	22166940	CNVD
Abnormal phenotypes	18644119	CNVD
Non-syndromic sensorineural hearing loss	22570644	CNVD
Bladder cancer	21909424	CNVD
Cancer	21183584	CNVD
Autism	20808228	CNVD
Sezary syndrome	18413736	CNVD
Multiple myeloma	17550852	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	22495309	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD

Chromatin state (count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:16961000-16973400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr7:16963200-16972400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
3	chr7:16963200-16973600	Weak transcription	Small Intestine	intestine
4	chr7:16964800-16969600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:16965600-16970200	Enhancers	Stomach Mucosa	stomach
6	chr7:16966000-16968800	Weak transcription	Fetal Thymus	thymus
7	chr7:16966000-16968800	Weak transcription	Thymus	Thymus
8	chr7:16966400-16968800	Weak transcription	Rectal Mucosa Donor 29	rectum
9	chr7:16966600-16973200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr7:16966800-16974800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:16967000-16968800	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr7:16967200-16977600	Weak transcription	Gastric	stomach
13	chr7:16967600-16968800	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr7:16967600-16974200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr7:16967800-16974200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr7:16968000-16974000	Weak transcription	NHEK	skin
17	chr7:16968200-16973000	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr7:16968400-16968800	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr7:16968400-16970800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr7:16968400-16973000	Enhancers	Primary T cells from cord blood	blood
21	chr7:16968400-16973200	Enhancers	Primary B cells from cord blood	blood
22	chr7:16968600-16968800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
23	chr7:16968600-16969000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
24	chr7:16968600-16970400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr7:16968600-16970800	Enhancers	Primary B cells from peripheral blood	blood
26	chr7:16968600-16971600	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr7:16968600-16972000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr7:16968800-16969000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
29	chr7:16968800-16969000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr7:16968800-16969000	Enhancers	Sigmoid Colon	Sigmoid Colon
31	chr7:16968800-16969000	Enhancers	GM12878-XiMat	blood
32	chr7:16968800-16969200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr7:16968800-16969200	Enhancers	Primary T helper naive cells from peripheral blood	blood
34	chr7:16968800-16969200	Enhancers	Rectal Mucosa Donor 29	rectum
35	chr7:16968800-16969800	Enhancers	Rectal Mucosa Donor 31	rectum
36	chr7:16968800-16970000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr7:16968800-16970200	Enhancers	Primary neutrophils fromperipheralblood	blood
38	chr7:16968800-16971200	Enhancers	Primary T helper cells fromperipheralblood	blood
39	chr7:16968800-16971400	Enhancers	Primary monocytes fromperipheralblood	blood
40	chr7:16968800-16971400	Enhancers	Fetal Thymus	thymus
41	chr7:16968800-16974800	Enhancers	Thymus	Thymus
42	chr7:16969000-16969200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr7:16969000-16969200	Enhancers	Primary T killer memory cells from peripheral blood	blood
44	chr7:16969000-16969400	Weak transcription	Sigmoid Colon	Sigmoid Colon
45	chr7:16969000-16970000	Enhancers	Primary hematopoietic stem cells	blood
46	chr7:16969000-16970000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
47	chr7:16969000-16970000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr7:16969200-16970000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:16969200-16970200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr7:16969200-16970200	Weak transcription	Primary T helper naive cells from peripheral blood	blood

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