Variant report

Variant	nsv1011175
Chromosome Location	chr3:141904977-142076561
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1911)
CpG islands
(count:856)
Chromatin interactive
region (count:103)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1911 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
2	ARID3A	chr3:142034796-142035079	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
5	ARID3A	chr3:142034735-142035065	K562	blood:	n/a	n/a
6	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
7	ARID3A	chr3:142037995-142038366	K562	blood:	n/a	n/a
8	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
9	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
10	ATF1	chr3:142038012-142038223	K562	blood:	n/a	n/a
11	ATF1	chr3:142026474-142026530	K562	blood:	n/a	n/a
12	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
13	ATF1	chr3:142034743-142035113	K562	blood:	n/a	n/a
14	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
15	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
17	ATF3	chr3:142034698-142035057	K562	blood:	n/a	n/a
18	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
20	BACH1	chr3:142037969-142038499	K562	blood:	n/a	n/a
21	BACH1	chr3:142037995-142038332	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
23	BATF	chr3:142074556-142074897	GM12878	blood:	n/a	n/a
24	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
25	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
26	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
27	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
29	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
30	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
31	BHLHE40	chr3:142066400-142066735	K562	blood:	n/a	n/a
32	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
34	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
35	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr3:141994588-141995155	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
38	CBX3	chr3:141972002-141972303	K562	blood:	n/a	n/a
39	CBX3	chr3:141974109-141974466	K562	blood:	n/a	n/a
40	CBX3	chr3:142003802-142004433	K562	blood:	n/a	n/a
41	CBX3	chr3:141998807-141999224	K562	blood:	n/a	n/a
42	CBX3	chr3:141972050-141972272	K562	blood:	n/a	n/a
43	CBX3	chr3:141951133-141951609	K562	blood:	n/a	n/a
44	CBX3	chr3:141951267-141951575	K562	blood:	n/a	n/a
45	CBX3	chr3:141998618-141999310	K562	blood:	n/a	n/a
46	CBX3	chr3:142006799-142007385	HCT-116	colon:	n/a	n/a
47	CBX3	chr3:142003887-142004274	K562	blood:	n/a	n/a
48	CBX3	chr3:141943716-141945024	K562	blood:	n/a	n/a
49	CCNT2	chr3:141941669-141942029	K562	blood:	n/a	n/a
50	CCNT2	chr3:142034749-142035043	K562	blood:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141944519-141944569	ovcar-3	ovarian:	n/a
2	chr3:141944318-141944368	HRCEpiC	kidney:	n/a
3	chr3:141944519-141944569	ovcar-3	ovarian:	n/a
4	chr3:141944318-141944368	HRCEpiC	kidney:	n/a
5	chr3:141943895-141943945	ovcar-3	ovarian:	n/a
6	chr3:141944620-141944670	IMR90	lung:	fetal
7	chr3:141941279-141941329	AoSMC	blood vessel:	n/a
8	chr3:141941279-141941329	HCPEpiC	choroid plexus:	n/a
9	chr3:141944519-141944569	GM06990	blood:	n/a
10	chr3:141945790-141945840	HCT-116	colon:	n/a
11	chr3:141945790-141945840	H1-hESC	embryonic stem cell:	embryo
12	chr3:141995701-141995751	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:141945703-141945753	U87	brain:	n/a
14	chr3:141945703-141945753	T-47D	breast:	n/a
15	chr3:141995701-141995751	HRCEpiC	kidney:	n/a
16	chr3:141945703-141945753	NHBE	bronchial:	n/a
17	chr3:141945790-141945840	HCM	heart:	n/a
18	chr3:141995701-141995751	NB4	blood:	n/a
19	chr3:141944344-141944394	RPTEC	kidney:	n/a
20	chr3:141944318-141944368	GM12878	blood:	n/a
21	chr3:141944318-141944368	AG04449	skin:	fetal
22	chr3:141944077-141944127	IMR90	lung:	fetal
23	chr3:141944300-141944350	SK-N-MC	brain:	n/a
24	chr3:141944620-141944670	AG09309	skin:	n/a
25	chr3:141945703-141945753	HEK293	kidney:	embryo
26	chr3:142027066-142027116	PANC-1	pancreas:	n/a
27	chr3:141928789-141928839	AG04450	lung:	fetal
28	chr3:141944077-141944127	AG10803	skin:	n/a
29	chr3:141928789-141928839	NHDF-neo	bronchial:	n/a
30	chr3:141944318-141944368	BJ	skin:	n/a
31	chr3:141944620-141944670	GM12891	blood:	n/a
32	chr3:141941279-141941329	SK-N-MC	brain:	n/a
33	chr3:141928789-141928839	NH-A	brain:	n/a
34	chr3:141944516-141944566	U87	brain:	n/a
35	chr3:141941279-141941329	HEK293	kidney:	embryo
36	chr3:141944344-141944394	HCM	heart:	n/a
37	chr3:142027066-142027116	T-47D	breast:	n/a
38	chr3:141945703-141945753	HUVEC	blood vessel:	n/a
39	chr3:141944318-141944368	Hepatocyte	liver:	n/a
40	chr3:141944344-141944394	HRE	kidney:	n/a
41	chr3:141928789-141928839	SAEC	small airway:	n/a
42	chr3:141945703-141945753	PrEC	prostate:	n/a
43	chr3:141944519-141944569	MCF10A-Er-Src	breast:	n/a
44	chr3:141928789-141928839	HL-60	blood:	n/a
45	chr3:141944516-141944566	Jurkat	blood:	n/a
46	chr3:141944519-141944569	PANC-1	pancreas:	n/a
47	chr3:141944318-141944368	PrEC	prostate:	n/a
48	chr3:141944620-141944670	HRCEpiC	kidney:	n/a
49	chr3:141928789-141928839	ProgFib	skin:	n/a
50	chr3:141941279-141941329	NT2-D1	testis:	n/a

(count:103 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
2	chr3:141746412..141748907-chr3:141928677..141931000,3	K562	blood:
3	chr3:23982130..23982921-chr3:141945206..141945893,2	MCF-7	breast:
4	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
5	chr3:141918309..141919900-chr3:141924207..141926926,2	MCF-7	breast:
6	chr3:142064702..142067188-chr3:142070699..142072268,2	K562	blood:
7	chr3:141918175..141919992-chr3:141942842..141946920,3	MCF-7	breast:
8	chr3:141739542..141742444-chr3:142003603..142005533,2	K562	blood:
9	chr3:142028519..142033203-chr3:142033786..142039324,7	K562	blood:
10	chr3:141918309..141919900-chr3:141924207..141926926,2	MCF-7	breast:
11	chr3:141943937..141944882-chr5:32585069..32586043,2	Hela-S3	cervix:
12	chr3:142048008..142050372-chr3:142051605..142054312,2	K562	blood:
13	chr3:141942954..141945885-chr3:141988032..141991755,3	MCF-7	breast:
14	chr3:141844721..141845463-chr3:141945183..141945790,2	MCF-7	breast:
15	chr3:141928249..141931424-chr3:141932973..141936618,4	K562	blood:
16	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
17	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
18	chr3:141918898..141921887-chr3:141933656..141936243,2	K562	blood:
19	chr3:141941642..141944817-chr3:141944838..141947150,3	K562	blood:
20	chr3:141681160..141682062-chr3:141998578..141999511,3	K562	blood:
21	chr3:142071094..142074933-chr3:142076608..142079513,3	MCF-7	breast:
22	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
23	chr3:142026133..142029209-chr3:142034990..142037893,3	MCF-7	breast:
24	chr3:141899683..141900200-chr3:141998508..141999054,2	K562	blood:
25	chr3:141941960..141945693-chr3:142033521..142037066,3	K562	blood:
26	chr3:141914914..141916949-chr3:141917367..141920269,2	K562	blood:
27	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
28	chr3:141844475..141845747-chr3:141998357..141999102,5	K562	blood:
29	chr3:141939985..141942934-chr3:141962121..141964269,2	K562	blood:
30	chr3:141944137..141946098-chr3:141949464..141952210,3	K562	blood:
31	chr3:142028519..142031113-chr3:142035238..142036947,2	K562	blood:
32	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
33	chr3:141745328..141748975-chr3:142003993..142005586,3	K562	blood:
34	chr3:141927414..141929752-chr3:141932597..141934385,2	MCF-7	breast:
35	chr3:141733456..141735928-chr3:141995928..141997484,2	K562	blood:
36	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:
37	chr3:141998539..142000204-chr3:142002540..142004917,2	K562	blood:
38	chr3:141927414..141929752-chr3:141932597..141934385,2	MCF-7	breast:
39	chr3:141921447..141923041-chr3:141938532..141940338,2	K562	blood:
40	chr3:141940937..141945863-chr3:141947298..141949257,5	K562	blood:
41	chr17:62222919..62223709-chr3:141944062..141944934,2	HCT-116	colon:
42	chr3:141939985..141942934-chr3:141962121..141964269,2	K562	blood:
43	chr3:141944430..141944948-chr7:35839962..35840580,2	Hela-S3	cervix:
44	chr3:141921447..141923041-chr3:141938532..141940338,2	K562	blood:
45	chr17:80184285..80186683-chr3:141942385..141945027,2	MCF-7	breast:
46	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
47	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
48	chr3:142047932..142050372-chr3:142051605..142055072,3	K562	blood:
49	chr3:142025469..142027957-chr3:142037548..142040461,2	K562	blood:
50	chr3:141944534..141946087-chr3:141987477..141990045,2	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	XRN1	hsa-miR-335-5p	chr3:142025482-142025506
2	XRN1	hsa-miR-10a-5p	chr3:142029586-142029608
3	XRN1	hsa-miR-10a-5p	chr3:142029592-142029585
4	XRN1	hsa-let-7b-5p	chr3:142030132-142030126

Variant related genes	Relation type
GK5	TF binding region
XRN1	TF binding region
GK5	CpG island
XRN1	CpG island
ENSG00000272565	chromatin interactions
ENSG00000253806	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000202444	chromatin interactions
ENSG00000175066	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000114127	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000113387	chromatin interactions
ENSG00000160183	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000130193	chromatin interactions
ENSG00000228878	chromatin interactions
ENSG00000266402	chromatin interactions

Extended variants
information (count: 5273 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:5273 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6440065	chr3:141904977-141904978	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs370693920	chr3:141905005-141905006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs559160501	chr3:141905071-141905072	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs138022219	chr3:141905074-141905075	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142593210	chr3:141905107-141905108	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs376391725	chr3:141905124-141905125	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532939410	chr3:141905137-141905138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs373740674	chr3:141905151-141905152	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545334466	chr3:141905181-141905182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115640539	chr3:141905216-141905217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9837628	chr3:141905253-141905254	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9857725	chr3:141905259-141905260	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs9857726	chr3:141905261-141905262	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs375379632	chr3:141905271-141905272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142154007	chr3:141905278-141905279	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528159271	chr3:141905286-141905287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs369098751	chr3:141905299-141905300	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs77132218	chr3:141905345-141905346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568640893	chr3:141905378-141905379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs191746628	chr3:141905414-141905415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs6799018	chr3:141905416-141905417	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs557685987	chr3:141905418-141905419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71629531	chr3:141905457-141905458	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs547999555	chr3:141905463-141905464	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs569407814	chr3:141905465-141905466	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372184440	chr3:141905472-141905473	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536673627	chr3:141905524-141905525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs566390078	chr3:141905527-141905528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188456621	chr3:141905550-141905551	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs111691591	chr3:141905583-141905584	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572889503	chr3:141905588-141905589	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534058792	chr3:141905596-141905597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558622806	chr3:141905597-141905598	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6801532	chr3:141905611-141905612	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs181643270	chr3:141905620-141905621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs577160220	chr3:141905627-141905628	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs6764179	chr3:141905630-141905631	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs370414510	chr3:141905669-141905670	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs142987320	chr3:141905705-141905706	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs560901084	chr3:141905718-141905719	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs151124402	chr3:141905728-141905729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs113062785	chr3:141905736-141905737	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs546762077	chr3:141905752-141905753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529441521	chr3:141905753-141905754	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs564961869	chr3:141905763-141905764	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377487154	chr3:141905788-141905789	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140078073	chr3:141905824-141905825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550869059	chr3:141905829-141905830	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs569551893	chr3:141905884-141905885	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs541654586	chr3:141905897-141905898	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:56)

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
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	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
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:3197 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141868800-141943000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
2	chr3:141869000-141922200	Weak transcription	A549	lung
3	chr3:141869000-141926800	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr3:141880000-141906800	Strong transcription	Fetal Intestine Large	intestine
5	chr3:141880200-141906600	Strong transcription	Monocytes-CD14+_RO01746	blood
6	chr3:141881000-141920800	Weak transcription	Small Intestine	intestine
7	chr3:141881600-141922800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:141882000-141906800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr3:141883200-141906800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:141883600-141927200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr3:141886800-141906200	Weak transcription	Stomach Mucosa	stomach
12	chr3:141886800-141907400	Weak transcription	Fetal Heart	heart
13	chr3:141887000-141906800	Strong transcription	Muscle Satellite Cultured Cells	--
14	chr3:141888000-141943200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
15	chr3:141888200-141922600	Weak transcription	H9 Cell Line	embryonic stem cell
16	chr3:141888400-141922600	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr3:141888400-141927200	Weak transcription	GM12878-XiMat	blood
18	chr3:141888400-141930000	Weak transcription	Placenta Amnion	Placenta Amnion
19	chr3:141888600-141928600	Weak transcription	Brain Hippocampus Middle	brain
20	chr3:141889000-141943600	Weak transcription	Psoas Muscle	Psoas
21	chr3:141889200-141920800	Weak transcription	Brain Cingulate Gyrus	brain
22	chr3:141889200-141920800	Weak transcription	Spleen	Spleen
23	chr3:141889200-141922400	Weak transcription	Fetal Brain Male	brain
24	chr3:141889400-141922600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr3:141889400-141922800	Weak transcription	NHLF	lung
26	chr3:141889400-141926600	Weak transcription	Primary B cells from peripheral blood	blood
27	chr3:141889400-141928200	Weak transcription	HSMMtube	muscle
28	chr3:141889400-141928400	Weak transcription	HUVEC	blood vessel
29	chr3:141889400-141928600	Weak transcription	Brain Substantia Nigra	brain
30	chr3:141889600-141926600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr3:141890000-141920800	Weak transcription	Gastric	stomach
32	chr3:141890000-141920800	Weak transcription	Thymus	Thymus
33	chr3:141890000-141921000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr3:141890000-141922800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr3:141890000-141922800	Weak transcription	NHEK	skin
36	chr3:141890000-141929000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
37	chr3:141893800-141926600	Weak transcription	Primary T helper cells PMA-I stimulated	--
38	chr3:141896400-141916800	Weak transcription	HUES6 Cell Line	embryonic stem cell
39	chr3:141896400-141926600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr3:141896600-141905800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr3:141896600-141921200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr3:141896600-141930000	Weak transcription	Skeletal Muscle Male	skeletal muscle
43	chr3:141896600-141943200	Weak transcription	HMEC	breast
44	chr3:141898000-141922800	Weak transcription	NHDF-Ad	bronchial
45	chr3:141898800-141922600	Weak transcription	Hela-S3	cervix
46	chr3:141899200-141920000	Weak transcription	Placenta	Placenta
47	chr3:141899400-141906800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr3:141899600-141920800	Weak transcription	Pancreas	Pancrea
49	chr3:141899800-141907200	Weak transcription	Right Ventricle	heart
50	chr3:141899800-141916000	Weak transcription	Liver	Liver

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