Variant report

Variant	esv1799481
Chromosome Location	chr3:178733212-178782021
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:52)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

No data

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:178747112..178748794-chr3:179040862..179042416,2	K562	blood:
2	chr3:178744477..178746075-chr3:179040271..179042202,2	K562	blood:
3	chr3:178726976..178728535-chr3:178731027..178733316,2	K562	blood:
4	chr3:178743840..178745524-chr3:178976427..178980039,3	K562	blood:
5	chr3:178739768..178742264-chr3:178744553..178747173,2	K562	blood:
6	chr3:178743208..178744872-chr3:178748172..178749949,2	K562	blood:
7	chr3:178742128..178744484-chr3:178786941..178789605,2	MCF-7	breast:
8	chr3:178733361..178735780-chr3:178739021..178740577,2	K562	blood:
9	chr3:178741511..178744382-chr3:178747703..178750492,2	K562	blood:
10	chr3:178733040..178733565-chr3:179039064..179039702,4	K562	blood:
11	chr3:178770602..178773150-chr3:178777217..178780693,3	K562	blood:
12	chr3:178746545..178749111-chr3:178752950..178755283,2	MCF-7	breast:
13	chr3:178734194..178736320-chr3:178865690..178868620,2	K562	blood:
14	chr3:178733066..178734018-chr3:178786781..178787974,3	MCF-7	breast:
15	chr3:178741511..178744382-chr3:178747703..178750492,2	K562	blood:
16	chr3:178780357..178782332-chr3:178782506..178785505,2	MCF-7	breast:
17	chr3:178770602..178773150-chr3:178777217..178780693,3	K562	blood:
18	chr3:178770676..178772962-chr3:178864857..178866816,2	K562	blood:
19	chr3:178732951..178734901-chr3:178785761..178787497,2	K562	blood:
20	chr3:178733167..178734215-chr3:178815745..178816834,3	MCF-7	breast:
21	chr3:178751571..178753559-chr3:178782217..178784298,2	K562	blood:
22	chr3:178732002..178735693-chr3:178752423..178754842,3	K562	blood:
23	chr3:178746545..178749111-chr3:178752950..178755283,2	MCF-7	breast:
24	chr3:178743217..178745083-chr3:178864764..178866616,2	K562	blood:
25	chr3:178741058..178743011-chr3:178747228..178749203,2	K562	blood:
26	chr3:178736144..178738008-chr3:178740817..178744400,3	K562	blood:
27	chr3:178778004..178779935-chr3:178784372..178786776,2	MCF-7	breast:
28	chr3:178732002..178735693-chr3:178752423..178754842,3	K562	blood:
29	chr3:178781504..178783011-chr3:178869309..178871100,2	K562	blood:
30	chr3:178731577..178735974-chr3:179037653..179042692,7	K562	blood:
31	chr3:178749053..178750789-chr3:178751564..178754052,2	MCF-7	breast:
32	chr3:178739768..178742264-chr3:178744553..178747173,2	K562	blood:
33	chr3:178733385..178733982-chr3:179276676..179277195,2	K562	blood:
34	chr3:178733091..178733955-chr3:179038794..179040035,7	MCF-7	breast:
35	chr3:178733361..178735780-chr3:178739021..178740577,2	K562	blood:
36	chr3:178732575..178734006-chr3:179033177..179034478,10	K562	blood:
37	chr3:178780519..178783087-chr3:178791350..178793561,2	MCF-7	breast:
38	chr3:178754772..178756470-chr3:179039560..179042041,2	MCF-7	breast:
39	chr3:178735573..178738499-chr3:179040054..179042168,2	MCF-7	breast:
40	chr3:178781078..178783902-chr3:178788373..178789943,2	MCF-7	breast:
41	chr3:178733027..178734649-chr3:178978479..178979997,2	K562	blood:
42	chr3:178733474..178734188-chr3:179040675..179041525,2	MCF-7	breast:
43	chr3:178736144..178738008-chr3:178740817..178744400,3	K562	blood:
44	chr3:178743208..178744872-chr3:178748172..178749949,2	K562	blood:
45	chr3:178763837..178765875-chr3:178785002..178787931,2	K562	blood:
46	chr3:178737773..178739885-chr3:179056978..179059649,2	K562	blood:
47	chr3:178753336..178756153-chr3:178870610..178872335,2	K562	blood:
48	chr3:178577358..178579188-chr3:178747184..178750158,2	K562	blood:
49	chr3:178733073..178733959-chr3:178864672..178865566,2	MCF-7	breast:
50	chr3:178734474..178738470-chr3:179037032..179039856,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNMB2-9	chr3:178739877-178739975	l_2535_chr3:178642424-178743704_colon
2	lnc-KCNMB2-9	chr3:178743681-178743704	l_2535_chr3:178642424-178743704_colon
3	lnc-ZMAT3-4	chr3:178735011-178737876	NONHSAT093385

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ZMAT3	hsa-miR-192-5p	chr3:178742596-178742616
2	ZMAT3	hsa-miR-215-5p	chr3:178742596-178742616
3	ZMAT3	hsa-miR-215-5p	chr3:178742184-178742202
4	ZMAT3	hsa-miR-192-5p	chr3:178742184-178742202

Variant related genes	Relation type
ENSG00000172667	chromatin interactions
ENSG00000121864	chromatin interactions
ENSG00000260743	chromatin interactions
ENSG00000121879	chromatin interactions
ENSG00000237978	chromatin interactions
ENSG00000171121	chromatin interactions
ENSG00000240429	chromatin interactions
ENSG00000229102	chromatin interactions

Extended variants
information (count: 1755 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:1755 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4579062	chr3:178733212-178733213	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs532784722	chr3:178733244-178733245	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs562556754	chr3:178733259-178733260	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191509556	chr3:178733263-178733264	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs183607478	chr3:178733288-178733289	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs189502768	chr3:178733299-178733300	Enhancers Weak transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs569406568	chr3:178733457-178733458	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs527604159	chr3:178733487-178733488	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs182041600	chr3:178733517-178733518	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs373716601	chr3:178733567-178733568	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs570578835	chr3:178733728-178733729	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs539600419	chr3:178733847-178733848	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs558659251	chr3:178733868-178733869	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs568998518	chr3:178733886-178733887	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs369156333	chr3:178733893-178733894	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs201789792	chr3:178733913-178733914	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373420591	chr3:178733933-178733934	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs185532506	chr3:178733944-178733945	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs574735017	chr3:178734107-178734108	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs7639391	chr3:178734122-178734123	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs554417363	chr3:178734139-178734140	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs577400317	chr3:178734151-178734152	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs546369449	chr3:178734172-178734173	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562620214	chr3:178734205-178734206	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs576352270	chr3:178734249-178734250	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs576209022	chr3:178734275-178734276	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs541909264	chr3:178734399-178734400	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs561685052	chr3:178734425-178734426	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs527253847	chr3:178734429-178734430	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs535506379	chr3:178734446-178734447	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs547405092	chr3:178734481-178734482	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs190339158	chr3:178734550-178734551	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs181670713	chr3:178734622-178734623	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs147314600	chr3:178734637-178734638	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs569462825	chr3:178734687-178734688	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs548622055	chr3:178734711-178734712	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs34197799	chr3:178734733-178734734	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs537959088	chr3:178734766-178734767	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs140039666	chr3:178734812-178734813	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs76680043	chr3:178734813-178734814	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs370193583	chr3:178734846-178734847	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs572436872	chr3:178734924-178734925	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs112377982	chr3:178734930-178734931	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs554210162	chr3:178734938-178734939	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs149819534	chr3:178734966-178734967	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs144804888	chr3:178734971-178734972	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs556805854	chr3:178735033-178735034	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
48	rs186657195	chr3:178735051-178735052	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
49	rs191001350	chr3:178735060-178735061	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
50	rs561801985	chr3:178735075-178735076	Weak transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:77)

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	22032731	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
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Medulloblastoma	21163964	CNVD

Chromatin state (count:1273 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:178708800-178737800	Weak transcription	Colon Smooth Muscle	Colon
2	chr3:178716400-178755000	Weak transcription	Pancreas	Pancrea
3	chr3:178717400-178744400	Weak transcription	HMEC	breast
4	chr3:178719200-178737600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr3:178720400-178734200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr3:178720600-178737600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:178721400-178737800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr3:178721400-178738000	Weak transcription	Aorta	Aorta
9	chr3:178722200-178751600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:178723000-178733600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr3:178723400-178749800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr3:178723800-178754200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr3:178727800-178738000	Weak transcription	Fetal Heart	heart
14	chr3:178731200-178735200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:178731400-178744400	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chr3:178732600-178744200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr3:178732800-178738000	Weak transcription	Fetal Thymus	thymus
18	chr3:178733000-178733800	Enhancers	Dnd41	blood
19	chr3:178733000-178734200	Enhancers	Primary T cells from cord blood	blood
20	chr3:178733000-178735400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chr3:178733000-178735600	Enhancers	Primary T helper cells PMA-I stimulated	--
22	chr3:178733000-178738600	Weak transcription	NH-A	brain
23	chr3:178733200-178733400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr3:178733200-178733400	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr3:178733200-178733800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr3:178733200-178733800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr3:178733200-178733800	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr3:178733200-178733800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr3:178733200-178733800	Enhancers	Primary T regulatory cells fromperipheralblood	blood
30	chr3:178733200-178733800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
31	chr3:178733200-178733800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr3:178733200-178733800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:178733200-178733800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr3:178733200-178733800	Enhancers	Muscle Satellite Cultured Cells	--
35	chr3:178733200-178733800	Enhancers	Brain Hippocampus Middle	brain
36	chr3:178733200-178733800	Enhancers	Fetal Lung	lung
37	chr3:178733200-178733800	Enhancers	HSMMtube	muscle
38	chr3:178733200-178733800	Enhancers	K562	blood
39	chr3:178733200-178733800	Enhancers	NHDF-Ad	bronchial
40	chr3:178733200-178734000	Enhancers	Primary T killer memory cells from peripheral blood	blood
41	chr3:178733200-178734000	Genic enhancers	HSMM	muscle
42	chr3:178733200-178734200	Enhancers	GM12878-XiMat	blood
43	chr3:178733200-178735000	Enhancers	Primary T helper cells fromperipheralblood	blood
44	chr3:178733200-178735200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
45	chr3:178733200-178735800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr3:178733200-178736000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr3:178733200-178736000	Enhancers	Primary B cells from cord blood	blood
48	chr3:178733400-178733800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr3:178733400-178737600	Weak transcription	HUVEC	blood vessel
50	chr3:178733400-178751400	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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