Variant report

Variant	esv3499754
Chromosome Location	chr3:195601063-195603076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:366)
Chromatin interactive
region (count:7)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EGR1	chr3:195600823-195601106	K562	blood:	n/a	n/a
2	EGR1	chr3:195600855-195601090	K562	blood:	n/a	n/a
3	FOSL2	chr3:195600812-195601320	SK-N-SH	brain:	n/a	n/a
4	HCFC1	chr3:195602331-195604823	Hela-S3	cervix:	n/a	n/a
5	MAX	chr3:195602508-195602604	Hela-S3	cervix:	n/a	n/a
6	MAX	chr3:195601030-195601256	Hela-S3	cervix:	n/a	n/a
7	MAZ	chr3:195602587-195602590	Hela-S3	cervix:	n/a	n/a
8	MYC	chr3:195601104-195601173	MCF-7	breast:	n/a	n/a
9	NR3C1	chr3:195601355-195602368	A549	lung:	n/a	n/a
10	PAX5	chr3:195601526-195602400	GM12878	blood:	n/a	n/a
11	POLR2A	chr3:195602948-195603965	Hela-S3	cervix:	n/a	n/a
12	POLR2A	chr3:195602467-195604049	Hela-S3	cervix:	n/a	n/a
13	POLR2A	chr3:195601599-195602305	GM12878	blood:	n/a	n/a
14	POLR2A	chr3:195601125-195601126	Hela-S3	cervix:	n/a	n/a
15	POLR2A	chr3:195601015-195601133	Gliobla	brain:	n/a	n/a
16	POLR2A	chr3:195601101-195601119	Hela-S3	cervix:	n/a	n/a
17	POLR2A	chr3:195602596-195602633	K562	blood:	n/a	n/a
18	POLR2A	chr3:195600910-195601262	Hela-S3	cervix:	n/a	n/a
19	POLR2A	chr3:195600837-195601307	Hela-S3	cervix:	n/a	n/a
20	RCOR1	chr3:195602589-195602937	Hela-S3	cervix:	n/a	n/a
21	RFX5	chr3:195601044-195601143	HepG2	liver:	n/a	n/a
22	RFX5	chr3:195600998-195601190	Hela-S3	cervix:	n/a	n/a
23	SMARCB1	chr3:195602688-195604540	Hela-S3	cervix:	n/a	chr3:195603753-195603762
24	SMARCC1	chr3:195602803-195604082	Hela-S3	cervix:	n/a	chr3:195603753-195603762
25	SRF	chr3:195601395-195601614	GM12878	blood:	n/a	n/a
26	SRF	chr3:195601626-195601928	GM12878	blood:	n/a	n/a
27	SRF	chr3:195601935-195602121	GM12878	blood:	n/a	n/a
28	SRF	chr3:195602124-195602318	GM12878	blood:	n/a	n/a
29	TAF1	chr3:195601002-195601216	Hela-S3	cervix:	n/a	n/a
30	TCF3	chr3:195601604-195601928	GM12878	blood:	n/a	n/a
31	TCF3	chr3:195602012-195602344	GM12878	blood:	n/a	n/a
32	ZNF143	chr3:195602671-195602707	Hela-S3	cervix:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:195601381-195601431	HEEpiC	esophagus:	n/a
2	chr3:195602360-195602410	U87	brain:	n/a
3	chr3:195601155-195601205	NT2-D1	testis:	n/a
4	chr3:195601381-195601431	NH-A	brain:	n/a
5	chr3:195601381-195601431	H1-hESC	embryonic stem cell:	embryo
6	chr3:195602274-195602324	HRE	kidney:	n/a
7	chr3:195602323-195602373	BE2_C	brain:	n/a
8	chr3:195601155-195601205	HPAEpiC	pulmonary alveolar:	n/a
9	chr3:195602274-195602324	HRCEpiC	kidney:	n/a
10	chr3:195601155-195601205	SK-N-SH	brain:	n/a
11	chr3:195602274-195602324	NHDF-neo	bronchial:	n/a
12	chr3:195601155-195601205	HCPEpiC	choroid plexus:	n/a
13	chr3:195602360-195602410	SAEC	small airway:	n/a
14	chr3:195602274-195602324	PrEC	prostate:	n/a
15	chr3:195602323-195602373	PrEC	prostate:	n/a
16	chr3:195601155-195601205	SK-N-MC	brain:	n/a
17	chr3:195602274-195602324	SAEC	small airway:	n/a
18	chr3:195602274-195602324	HepG2	liver:	n/a
19	chr3:195601155-195601205	HMEC	breast:	n/a
20	chr3:195602360-195602410	MCF10A-Er-Src	breast:	n/a
21	chr3:195602274-195602324	BJ	skin:	n/a
22	chr3:195602360-195602410	AG04450	lung:	fetal
23	chr3:195601375-195601425	BJ	skin:	n/a
24	chr3:195602323-195602373	GM06990	blood:	n/a
25	chr3:195602360-195602410	HL-60	blood:	n/a
26	chr3:195601375-195601425	HRE	kidney:	n/a
27	chr3:195601155-195601205	CMK	blood:	n/a
28	chr3:195602360-195602410	HRPEpiC	eye:	n/a
29	chr3:195602360-195602410	BJ	skin:	n/a
30	chr3:195602323-195602373	MCF-7	breast:	n/a
31	chr3:195601155-195601205	ovcar-3	ovarian:	n/a
32	chr3:195601375-195601425	HepG2	liver:	n/a
33	chr3:195601375-195601425	NB4	blood:	n/a
34	chr3:195602274-195602324	AoSMC	blood vessel:	n/a
35	chr3:195601155-195601205	AG04449	skin:	fetal
36	chr3:195602323-195602373	GM12891	blood:	n/a
37	chr3:195601381-195601431	HPAEpiC	pulmonary alveolar:	n/a
38	chr3:195602360-195602410	Hela-S3	cervix:	n/a
39	chr3:195601375-195601425	HIPEpiC	eye:	n/a
40	chr3:195602360-195602410	AG09319	gingival:	n/a
41	chr3:195601375-195601425	HEEpiC	esophagus:	n/a
42	chr3:195602323-195602373	SK-N-MC	brain:	n/a
43	chr3:195601381-195601431	NHDF-neo	bronchial:	n/a
44	chr3:195602360-195602410	SK-N-MC	brain:	n/a
45	chr3:195602274-195602324	AG04450	lung:	fetal
46	chr3:195602323-195602373	HEEpiC	esophagus:	n/a
47	chr3:195602323-195602373	PFSK-1	brain:	n/a
48	chr3:195601381-195601431	HL-60	blood:	n/a
49	chr3:195601381-195601431	PrEC	prostate:	n/a
50	chr3:195602360-195602410	HCPEpiC	choroid plexus:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:195593301..195599220-chr3:195600993..195605430,9	MCF-7	breast:
2	chr3:195593517..195599119-chr3:195599450..195605625,8	MCF-7	breast:
3	chr3:195596788..195599344-chr3:195602164..195605260,3	K562	blood:
4	chr3:195602309..195605964-chr3:195633937..195639111,7	MCF-7	breast:
5	chr3:195601233..195610120-chr3:195632410..195638442,11	MCF-7	breast:
6	chr3:195600801..195603776-chr3:195621809..195623311,2	MCF-7	breast:
7	chr3:195601763..195604584-chr3:195636723..195640516,3	K562	blood:

No data

Variant related genes	Relation type
TNK2	TF binding region
TNK2	CpG island
ENSG00000061938	chromatin interactions
ENSG00000226155	chromatin interactions
ENSG00000224614	chromatin interactions

Extended variants
information (count: 159 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:159 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6793113	chr3:195601071-195601072	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543488294	chr3:195601092-195601093	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs567753583	chr3:195601103-195601104	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs182263574	chr3:195601155-195601156	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs541093606	chr3:195601161-195601162	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs559925224	chr3:195601185-195601186	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs186414107	chr3:195601189-195601190	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551951422	chr3:195601195-195601196	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs190043911	chr3:195601226-195601227	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs563245532	chr3:195601227-195601228	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs530426677	chr3:195601241-195601242	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs549539198	chr3:195601256-195601257	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs144587664	chr3:195601268-195601269	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs535557972	chr3:195601298-195601299	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs547471690	chr3:195601302-195601303	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs73205792	chr3:195601306-195601307	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs74555607	chr3:195601321-195601322	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs180688260	chr3:195601327-195601328	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs576694192	chr3:195601347-195601348	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs537723373	chr3:195601348-195601349	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs144986514	chr3:195601363-195601364	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs112914538	chr3:195601374-195601375	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs113055553	chr3:195601375-195601376	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs111626462	chr3:195601386-195601387	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs573659206	chr3:195601391-195601392	Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs570644429	chr3:195601412-195601413	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs541132350	chr3:195601413-195601414	Weak transcription Strong transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs11714769	chr3:195601448-195601449	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs200006490	chr3:195601451-195601452	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs553098907	chr3:195601458-195601459	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs28706969	chr3:195601476-195601477	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs55855604	chr3:195601482-195601483	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs13066070	chr3:195601493-195601494	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs545712804	chr3:195601517-195601518	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs76674096	chr3:195601520-195601521	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs75701106	chr3:195601524-195601525	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs564283639	chr3:195601537-195601538	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs13091590	chr3:195601577-195601578	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs13066245	chr3:195601578-195601579	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs201063258	chr3:195601584-195601585	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs11720562	chr3:195601585-195601586	Weak transcription Strong transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs28491933	chr3:195601613-195601614	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs11714830	chr3:195601622-195601623	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs531530269	chr3:195601623-195601624	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs543665007	chr3:195601626-195601627	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs369023319	chr3:195601653-195601654	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs60500503	chr3:195601666-195601667	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs60933312	chr3:195601697-195601698	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs58347397	chr3:195601714-195601715	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs561535123	chr3:195601716-195601717	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:195578400-195604800	Weak transcription	GM12878-XiMat	blood
2	chr3:195586800-195603200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr3:195586800-195608600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr3:195587000-195603200	Weak transcription	Primary B cells from cord blood	blood
5	chr3:195587000-195603800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr3:195587400-195604800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr3:195589000-195612000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr3:195589400-195621800	Weak transcription	Small Intestine	intestine
9	chr3:195589800-195616200	Strong transcription	Primary neutrophils fromperipheralblood	blood
10	chr3:195589800-195618800	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr3:195589800-195619600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:195590000-195607200	Strong transcription	Thymus	Thymus
13	chr3:195590000-195607400	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr3:195590000-195615600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
15	chr3:195590200-195601600	Strong transcription	Primary T cells from cord blood	blood
16	chr3:195590200-195604000	Strong transcription	Monocytes-CD14+_RO01746	blood
17	chr3:195590200-195607400	Strong transcription	Primary T helper cells fromperipheralblood	blood
18	chr3:195590200-195615800	Strong transcription	Primary monocytes fromperipheralblood	blood
19	chr3:195590400-195602600	Weak transcription	K562	blood
20	chr3:195590400-195603000	Strong transcription	Fetal Intestine Small	intestine
21	chr3:195590400-195604600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr3:195590600-195601200	Strong transcription	Brain Germinal Matrix	brain
23	chr3:195590600-195604800	Weak transcription	NHDF-Ad	bronchial
24	chr3:195590600-195617000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:195591000-195603200	Weak transcription	Psoas Muscle	Psoas
26	chr3:195592000-195607000	Strong transcription	Lung	lung
27	chr3:195592200-195601200	Strong transcription	Adipose Nuclei	Adipose
28	chr3:195592200-195601400	Strong transcription	Cortex derived primary cultured neurospheres	brain
29	chr3:195592200-195615800	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:195592200-195616200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr3:195592400-195601200	Strong transcription	Esophagus	oesophagus
32	chr3:195592400-195601600	Strong transcription	Liver	Liver
33	chr3:195592400-195607600	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
34	chr3:195592600-195601400	Strong transcription	Fetal Intestine Large	intestine
35	chr3:195592600-195601600	Strong transcription	Primary T helper cells PMA-I stimulated	--
36	chr3:195592600-195607200	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr3:195592800-195601400	Strong transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr3:195593200-195601200	Strong transcription	Primary T cells fromperipheralblood	blood
39	chr3:195593200-195601600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
40	chr3:195593200-195607200	Strong transcription	Fetal Thymus	thymus
41	chr3:195593600-195601200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr3:195594200-195602600	Weak transcription	Rectal Mucosa Donor 31	rectum
43	chr3:195595000-195604800	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr3:195595600-195608800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr3:195595600-195618800	Weak transcription	Fetal Kidney	kidney
46	chr3:195596600-195603600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr3:195597400-195611800	Strong transcription	Fetal Stomach	stomach
48	chr3:195597600-195604200	Weak transcription	H1 Cell Line	embryonic stem cell
49	chr3:195597600-195604800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr3:195597800-195602400	Weak transcription	Duodenum Smooth Muscle	Duodenum

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