Variant report

Variant	esv3450350
Chromosome Location	chr3:195684355-195688653
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:97)
CpG islands
(count:122)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:97 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:195687778-195688031	K562	blood:	n/a	n/a
2	BATF	chr3:195688640-195688926	GM12878	blood:	n/a	n/a
3	CBX3	chr3:195687930-195689486	K562	blood:	n/a	n/a
4	CTCF	chr3:195686747-195686794	Kidney_OC	kidney:	n/a	n/a
5	EBF1	chr3:195685670-195685963	GM12878	blood:	n/a	n/a
6	EGR1	chr3:195687834-195688183	K562	blood:	n/a	n/a
7	EGR1	chr3:195687842-195688257	K562	blood:	n/a	n/a
8	FOSL2	chr3:195686604-195686964	HepG2	liver:	n/a	n/a
9	FOSL2	chr3:195687640-195689431	HepG2	liver:	n/a	n/a
10	FOXA1	chr3:195686597-195686952	HepG2	liver:	n/a	n/a
11	GATA2	chr3:195688610-195688854	K562	blood:	n/a	n/a
12	HEY1	chr3:195688606-195688856	HepG2	liver:	n/a	n/a
13	HEY1	chr3:195686686-195687079	HepG2	liver:	n/a	n/a
14	IRF1	chr3:195688229-195688520	K562	blood:	n/a	n/a
15	MAX	chr3:195685786-195685960	NB4	blood:	n/a	n/a
16	NR2F2	chr3:195687758-195688358	K562	blood:	n/a	n/a
17	PAX5	chr3:195688612-195688944	GM12878	blood:	n/a	n/a
18	PAX5	chr3:195688478-195689132	GM12878	blood:	n/a	n/a
19	PAX5	chr3:195687790-195687953	GM12878	blood:	n/a	n/a
20	PAX5	chr3:195688591-195688981	GM12878	blood:	n/a	n/a
21	PAX5	chr3:195688072-195688438	GM12878	blood:	n/a	n/a
22	PBX3	chr3:195687744-195687998	GM12878	blood:	n/a	n/a
23	PBX3	chr3:195688647-195689055	GM12878	blood:	n/a	n/a
24	PBX3	chr3:195688141-195688258	GM12878	blood:	n/a	n/a
25	PBX3	chr3:195688309-195688497	GM12878	blood:	n/a	n/a
26	POLR2A	chr3:195687712-195687873	K562	blood:	n/a	n/a
27	POLR2A	chr3:195687834-195688508	K562	blood:	n/a	n/a
28	POLR2A	chr3:195688095-195688499	HepG2	liver:	n/a	n/a
29	POLR2A	chr3:195688616-195689015	HepG2	liver:	n/a	n/a
30	POLR2A	chr3:195686557-195686760	GM12878	blood:	n/a	n/a
31	POLR2A	chr3:195687609-195688041	GM12878	blood:	n/a	n/a
32	POLR2A	chr3:195688627-195688642	Hela-S3	cervix:	n/a	n/a
33	POLR2A	chr3:195687751-195688503	GM12878	blood:	n/a	n/a
34	POLR2A	chr3:195687625-195689464	GM12891	blood:	n/a	n/a
35	POLR2A	chr3:195687586-195689833	GM12892	blood:	n/a	n/a
36	POLR2A	chr3:195687677-195688534	PANC-1	pancreas:	n/a	n/a
37	POLR2A	chr3:195688202-195689141	Hela-S3	cervix:	n/a	n/a
38	POLR2A	chr3:195687793-195687938	HepG2	liver:	n/a	n/a
39	POLR2A	chr3:195687561-195689226	PANC-1	pancreas:	n/a	n/a
40	POLR2A	chr3:195686459-195686574	HepG2	liver:	n/a	n/a
41	POLR2A	chr3:195688263-195688501	ECC-1	luminal epithelium:	n/a	n/a
42	POLR2A	chr3:195685385-195685964	SK-N-MC	brain:	n/a	n/a
43	POLR2A	chr3:195688219-195689233	GM12878	blood:	n/a	n/a
44	POLR2A	chr3:195687721-195689344	GM12892	blood:	n/a	n/a
45	POLR2A	chr3:195687541-195688784	SK-N-MC	brain:	n/a	n/a
46	POLR2A	chr3:195687835-195688228	U87	brain:	n/a	n/a
47	POLR2A	chr3:195685489-195685700	H1-hESC	embryonic stem cell:	n/a	n/a
48	POLR2A	chr3:195688126-195688482	GM12878	blood:	n/a	n/a
49	POLR2A	chr3:195687732-195688693	K562	blood:	n/a	n/a
50	POLR2A	chr3:195685829-195685843	GM12878	blood:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195688021-195688071	MCF-7	breast:	n/a
2	chr3:195688021-195688071	GM06990	blood:	n/a
3	chr3:195687741-195687791	HIPEpiC	eye:	n/a
4	chr3:195688021-195688071	AG09309	skin:	n/a
5	chr3:195687741-195687791	HMEC	breast:	n/a
6	chr3:195687741-195687791	GM12878	blood:	n/a
7	chr3:195688021-195688071	AoSMC	blood vessel:	n/a
8	chr3:195688021-195688071	Caco-2	colon:	n/a
9	chr3:195688021-195688071	A549	lung:	n/a
10	chr3:195687741-195687791	SK-N-SH_RA	brain:	n/a
11	chr3:195687741-195687791	ECC-1	luminal epithelium:	n/a
12	chr3:195688021-195688071	U87	brain:	n/a
13	chr3:195688021-195688071	HUVEC	blood vessel:	n/a
14	chr3:195688021-195688071	Hela-S3	cervix:	n/a
15	chr3:195688021-195688071	HL-60	blood:	n/a
16	chr3:195687741-195687791	ovcar-3	ovarian:	n/a
17	chr3:195687741-195687791	AG04450	lung:	fetal
18	chr3:195687741-195687791	T-47D	breast:	n/a
19	chr3:195687741-195687791	HCPEpiC	choroid plexus:	n/a
20	chr3:195688021-195688071	SK-N-SH_RA	brain:	n/a
21	chr3:195688021-195688071	HEEpiC	esophagus:	n/a
22	chr3:195687741-195687791	K562	blood:	n/a
23	chr3:195687741-195687791	HCM	heart:	n/a
24	chr3:195687741-195687791	IMR90	lung:	fetal
25	chr3:195688021-195688071	HCPEpiC	choroid plexus:	n/a
26	chr3:195688021-195688071	SK-N-SH	brain:	n/a
27	chr3:195687741-195687791	AG09309	skin:	n/a
28	chr3:195688021-195688071	HRE	kidney:	n/a
29	chr3:195688021-195688071	Jurkat	blood:	n/a
30	chr3:195687741-195687791	SAEC	small airway:	n/a
31	chr3:195687741-195687791	GM12892	blood:	n/a
32	chr3:195688021-195688071	HRPEpiC	eye:	n/a
33	chr3:195687741-195687791	HRCEpiC	kidney:	n/a
34	chr3:195687741-195687791	MCF-7	breast:	n/a
35	chr3:195687741-195687791	U87	brain:	n/a
36	chr3:195687741-195687791	H1-hESC	embryonic stem cell:	embryo
37	chr3:195687741-195687791	NHBE	bronchial:	n/a
38	chr3:195687741-195687791	SK-N-MC	brain:	n/a
39	chr3:195688021-195688071	Hepatocyte	liver:	n/a
40	chr3:195688021-195688071	H1-hESC	embryonic stem cell:	embryo
41	chr3:195687741-195687791	HEK293	kidney:	embryo
42	chr3:195687741-195687791	MCF10A-Er-Src	breast:	n/a
43	chr3:195688021-195688071	ovcar-3	ovarian:	n/a
44	chr3:195687741-195687791	NB4	blood:	n/a
45	chr3:195688021-195688071	HCF	heart:	n/a
46	chr3:195687741-195687791	HRE	kidney:	n/a
47	chr3:195687741-195687791	Jurkat	blood:	n/a
48	chr3:195687741-195687791	NT2-D1	testis:	n/a
49	chr3:195687741-195687791	RPTEC	kidney:	n/a
50	chr3:195688021-195688071	IMR90	lung:	fetal

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:195416074..195419636-chr3:195682871..195685500,3	K562	blood:
2	chr3:195419233..195421889-chr3:195682348..195684419,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000260261	TF binding region
ENSG00000260261	CpG island
ENSG00000242086	chromatin interactions

Extended variants
information (count: 314 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:314 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76617921	chr3:195684363-195684364	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs575080320	chr3:195684364-195684365	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs112140651	chr3:195684369-195684370	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs74631636	chr3:195684374-195684375	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs536127502	chr3:195684400-195684401	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs3862279	chr3:195684418-195684419	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
7	rs145729389	chr3:195684430-195684431	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs368448085	chr3:195684431-195684432	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397894912	chr3:195684432-195684433	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs3081590	chr3:195684433-195684434	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548292935	chr3:195684447-195684448	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141554716	chr3:195684452-195684453	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs58330447	chr3:195684453-195684454	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547757037	chr3:195684459-195684460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs554222106	chr3:195684472-195684473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs191821895	chr3:195684485-195684486	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs183890720	chr3:195684486-195684487	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114693092	chr3:195684498-195684499	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs188891769	chr3:195684505-195684506	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs7371976	chr3:195684515-195684516	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7372331	chr3:195684523-195684524	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
22	rs529956064	chr3:195684535-195684536	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs541757295	chr3:195684559-195684560	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs562067053	chr3:195684561-195684562	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs527333230	chr3:195684562-195684563	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs551747654	chr3:195684567-195684568	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs111475386	chr3:195684587-195684588	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs112372218	chr3:195684599-195684600	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs370697935	chr3:195684600-195684601	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550370171	chr3:195684604-195684605	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191332818	chr3:195684643-195684644	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs200545377	chr3:195684650-195684651	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs536041366	chr3:195684669-195684670	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs140347796	chr3:195684676-195684677	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566371089	chr3:195684680-195684681	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs3103754	chr3:195684685-195684686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs539879194	chr3:195684701-195684702	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199963369	chr3:195684738-195684739	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs557823945	chr3:195684749-195684750	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs576505551	chr3:195684758-195684759	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs57326838	chr3:195684769-195684770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs3107712	chr3:195684770-195684771	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
43	rs574322162	chr3:195684772-195684773	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs372365489	chr3:195684835-195684836	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs140348097	chr3:195684847-195684848	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs370496274	chr3:195684850-195684851	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs367912853	chr3:195684851-195684852	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs182104153	chr3:195684854-195684855	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
49	rs61607848	chr3:195684860-195684861	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs35827076	chr3:195684876-195684877	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
Autism	19653912	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Prostate cancer	18632612	CNVD
Cervical cancer	21062161	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Austim spectrum disorder	21302340	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	16397240	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
speech impairment	20736978	CNVD
Intracranial aneurysm	16715129	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mental retardation	17124404	CNVD
Congenital anomalies of the kidney and urinary tract	20299530	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Neurodevelopmental disorder	16760732	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Autism	20970697	CNVD
Developmental delay	18471269	CNVD
Intellectual disability	22045946	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Ovarian cancer	20844748	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Uveal melanoma	20484589	CNVD
3q29 microdeletion syndrome	20500065	CNVD
Biliary cancer	20453639	CNVD
3q29 microdeletion syndrome	22283845	CNVD
3q29 microdeletion syndrome	21626679	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD

Chromatin state (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195659600-195685600	Weak transcription	Small Intestine	intestine
2	chr3:195665200-195691800	Weak transcription	HSMMtube	muscle
3	chr3:195665400-195685200	Weak transcription	Aorta	Aorta
4	chr3:195667400-195686200	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr3:195677800-195691800	Weak transcription	NHDF-Ad	bronchial
6	chr3:195678000-195696200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr3:195679000-195691600	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr3:195679000-195695800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr3:195681600-195685600	Weak transcription	Gastric	stomach
10	chr3:195681600-195691600	Weak transcription	Primary T cells from cord blood	blood
11	chr3:195681600-195696200	Weak transcription	Primary B cells from cord blood	blood
12	chr3:195681800-195685200	Weak transcription	Monocytes-CD14+_RO01746	blood
13	chr3:195681800-195685400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:195681800-195685400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:195681800-195685400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr3:195681800-195685400	Weak transcription	Brain Anterior Caudate	brain
17	chr3:195681800-195685400	Weak transcription	Brain Substantia Nigra	brain
18	chr3:195681800-195685600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr3:195681800-195685600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
20	chr3:195681800-195685600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
21	chr3:195681800-195685600	Weak transcription	Brain Cingulate Gyrus	brain
22	chr3:195681800-195685600	Weak transcription	Left Ventricle	heart
23	chr3:195681800-195685600	Weak transcription	Pancreas	Pancrea
24	chr3:195681800-195685600	Weak transcription	Stomach Smooth Muscle	stomach
25	chr3:195681800-195685600	Weak transcription	GM12878-XiMat	blood
26	chr3:195681800-195685800	Weak transcription	Colon Smooth Muscle	Colon
27	chr3:195681800-195685800	Weak transcription	NH-A	brain
28	chr3:195681800-195686000	Weak transcription	Duodenum Smooth Muscle	Duodenum
29	chr3:195681800-195686000	Weak transcription	HSMM	muscle
30	chr3:195681800-195686200	Weak transcription	Thymus	Thymus
31	chr3:195681800-195688200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr3:195681800-195688600	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr3:195681800-195688800	Weak transcription	Pancreatic Islets	Pancreatic Islet
34	chr3:195681800-195689400	Weak transcription	A549	lung
35	chr3:195681800-195691600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr3:195681800-195691600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:195681800-195691600	Weak transcription	Stomach Mucosa	stomach
38	chr3:195681800-195695600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
39	chr3:195681800-195696200	Weak transcription	HepG2	liver
40	chr3:195681800-195696400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr3:195681800-195696400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
42	chr3:195681800-195696800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
43	chr3:195682000-195685200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr3:195682000-195685600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr3:195682000-195685600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
46	chr3:195682000-195691600	Weak transcription	HMEC	breast
47	chr3:195682400-195685400	Weak transcription	Primary T helper cells fromperipheralblood	blood
48	chr3:195682400-195685400	Weak transcription	Duodenum Mucosa	Duodenum
49	chr3:195682400-195685400	Weak transcription	Ovary	ovary
50	chr3:195682400-195686000	Weak transcription	Rectal Smooth Muscle	rectum

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