Variant report

Variant	esv2751979
Chromosome Location	chr3:141853926-142015590
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2479)
CpG islands
(count:1344)
Chromatin interactive
region (count:114)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:2479 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:141868710-141868857	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:141944275-141944587	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:142004029-142004406	K562	blood:	n/a	n/a
4	ARID3A	chr3:141944333-141944542	K562	blood:	n/a	n/a
5	ARID3A	chr3:141941528-141942036	K562	blood:	n/a	n/a
6	ARID3A	chr3:141868086-141868286	HepG2	liver:	n/a	n/a
7	ATF1	chr3:141994868-141995043	K562	blood:	n/a	n/a
8	ATF1	chr3:142004039-142004362	K562	blood:	n/a	n/a
9	ATF1	chr3:141944202-141944637	K562	blood:	n/a	n/a
10	ATF2	chr3:141944124-141944603	GM12878	blood:	n/a	n/a
11	ATF2	chr3:141944313-141944572	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr3:141944306-141944624	K562	blood:	n/a	chr3:141944456-141944466
13	BACH1	chr3:141909646-141909689	K562	blood:	n/a	n/a
14	BACH1	chr3:141988570-141988640	K562	blood:	n/a	n/a
15	BACH1	chr3:141867733-141868966	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr3:141944121-141944594	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr3:141975772-141975937	GM12878	blood:	n/a	n/a
18	BCLAF1	chr3:141998835-141999218	GM12878	blood:	n/a	n/a
19	BCLAF1	chr3:141998774-141999206	GM12878	blood:	n/a	n/a
20	BCLAF1	chr3:141944193-141944635	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:141998901-141999171	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:141868133-141868604	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:141944084-141944604	HepG2	liver:	n/a	n/a
24	BHLHE40	chr3:141998833-141999090	HepG2	liver:	n/a	n/a
25	BHLHE40	chr3:141943947-141944618	K562	blood:	n/a	chr3:141944033-141944049
26	BHLHE40	chr3:141944144-141944582	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:141867704-141868571	HepG2	liver:	n/a	n/a
28	BHLHE40	chr3:141998848-141999153	K562	blood:	n/a	n/a
29	BRCA1	chr3:141933218-141933348	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr3:141944283-141944600	Hela-S3	cervix:	n/a	n/a
31	BRCA1	chr3:141867873-141868061	HepG2	liver:	n/a	n/a
32	BRCA1	chr3:141994588-141995155	Hela-S3	cervix:	n/a	n/a
33	CBX3	chr3:141974109-141974466	K562	blood:	n/a	n/a
34	CBX3	chr3:141868168-141868537	K562	blood:	n/a	n/a
35	CBX3	chr3:141943716-141945024	K562	blood:	n/a	n/a
36	CBX3	chr3:142006799-142007385	HCT-116	colon:	n/a	n/a
37	CBX3	chr3:141972050-141972272	K562	blood:	n/a	n/a
38	CBX3	chr3:141951267-141951575	K562	blood:	n/a	n/a
39	CBX3	chr3:141998618-141999310	K562	blood:	n/a	n/a
40	CBX3	chr3:141951133-141951609	K562	blood:	n/a	n/a
41	CBX3	chr3:141998807-141999224	K562	blood:	n/a	n/a
42	CBX3	chr3:141972002-141972303	K562	blood:	n/a	n/a
43	CBX3	chr3:142003887-142004274	K562	blood:	n/a	n/a
44	CBX3	chr3:142003802-142004433	K562	blood:	n/a	n/a
45	CCNT2	chr3:141867966-141868502	K562	blood:	n/a	chr3:141868472-141868481
46	CCNT2	chr3:141941669-141942029	K562	blood:	n/a	n/a
47	CCNT2	chr3:141943795-141944658	K562	blood:	n/a	n/a
48	CEBPB	chr3:141938972-141939000	K562	blood:	n/a	n/a
49	CEBPB	chr3:141995636-141995976	IMR90	lung:	n/a	n/a
50	CEBPB	chr3:141995688-141995913	Hela-S3	cervix:	n/a	n/a

(count:1344 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:141868612-141868662	AG04449	skin:	fetal
2	chr3:141871386-141871436	Hela-S3	cervix:	n/a
3	chr3:141868612-141868662	AG04449	skin:	fetal
4	chr3:141871386-141871436	Hela-S3	cervix:	n/a
5	chr3:141867862-141867912	ECC-1	luminal epithelium:	n/a
6	chr3:141944516-141944566	Caco-2	colon:	n/a
7	chr3:141945703-141945753	SAEC	small airway:	n/a
8	chr3:141944318-141944368	IMR90	lung:	fetal
9	chr3:141888226-141888276	SAEC	small airway:	n/a
10	chr3:141868459-141868509	CMK	blood:	n/a
11	chr3:141928789-141928839	K562	blood:	n/a
12	chr3:141868612-141868662	CMK	blood:	n/a
13	chr3:141868997-141869047	Hela-S3	cervix:	n/a
14	chr3:141995701-141995751	ovcar-3	ovarian:	n/a
15	chr3:141944077-141944127	AG09309	skin:	n/a
16	chr3:141868459-141868509	NB4	blood:	n/a
17	chr3:141944300-141944350	HEEpiC	esophagus:	n/a
18	chr3:141928789-141928839	HepG2	liver:	n/a
19	chr3:141868459-141868509	AG09319	gingival:	n/a
20	chr3:141868997-141869047	GM12892	blood:	n/a
21	chr3:141867862-141867912	HEEpiC	esophagus:	n/a
22	chr3:141944077-141944127	HEEpiC	esophagus:	n/a
23	chr3:141867994-141868044	NB4	blood:	n/a
24	chr3:141944318-141944368	Hepatocyte	liver:	n/a
25	chr3:141868459-141868509	HEK293	kidney:	embryo
26	chr3:141868612-141868662	GM19239	blood:	n/a
27	chr3:141944318-141944368	NHDF-neo	bronchial:	n/a
28	chr3:141944077-141944127	AoSMC	blood vessel:	n/a
29	chr3:141941279-141941329	HL-60	blood:	n/a
30	chr3:141877942-141877992	HNPCEpiC	eye:	n/a
31	chr3:141888226-141888276	HCF	heart:	n/a
32	chr3:141944620-141944670	HRE	kidney:	n/a
33	chr3:141944344-141944394	HIPEpiC	eye:	n/a
34	chr3:141871386-141871436	NT2-D1	testis:	n/a
35	chr3:141944519-141944569	SK-N-SH	brain:	n/a
36	chr3:141995701-141995751	NHBE	bronchial:	n/a
37	chr3:141943895-141943945	HCPEpiC	choroid plexus:	n/a
38	chr3:141945790-141945840	NHDF-neo	bronchial:	n/a
39	chr3:141868409-141868459	NB4	blood:	n/a
40	chr3:141995701-141995751	HL-60	blood:	n/a
41	chr3:141944519-141944569	IMR90	lung:	fetal
42	chr3:141877942-141877992	HCF	heart:	n/a
43	chr3:141867994-141868044	T-47D	breast:	n/a
44	chr3:141868459-141868509	GM12892	blood:	n/a
45	chr3:141945790-141945840	SK-N-MC	brain:	n/a
46	chr3:141944344-141944394	HUVEC	blood vessel:	n/a
47	chr3:141995701-141995751	SK-N-SH_RA	brain:	n/a
48	chr3:141944344-141944394	AG09319	gingival:	n/a
49	chr3:141944620-141944670	NHBE	bronchial:	n/a
50	chr3:141941279-141941329	SKMC	muscle:	n/a

(count:114 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr3:141866172..141869567-chr3:141870149..141874954,7	MCF-7	breast:
2	chr3:141919047..141920973-chr3:141943572..141945964,2	MCF-7	breast:
3	chr21:43815752..43816528-chr3:141944124..141945000,2	Hela-S3	cervix:
4	chr3:141986894..141989145-chr3:141996424..141998046,2	K562	blood:
5	chr17:62222919..62223709-chr3:141944062..141944934,2	HCT-116	colon:
6	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
7	chr3:141914914..141916949-chr3:141917367..141920269,2	K562	blood:
8	chr3:141888192..141890414-chr3:141943053..141945967,2	MCF-7	breast:
9	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
10	chr3:141916087..141917951-chr3:141939342..141941586,2	K562	blood:
11	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
12	chr3:141921447..141923041-chr3:141938532..141940338,2	K562	blood:
13	chr3:141941642..141944817-chr3:141944838..141947150,3	K562	blood:
14	chr3:141930773..141933744-chr3:141940549..141942064,2	MCF-7	breast:
15	chr3:141681127..141682067-chr3:141998956..141999598,2	MCF-7	breast:
16	chr3:141866276..141868412-chr3:141942932..141945800,2	MCF-7	breast:
17	chr3:141929745..141931253-chr3:141941462..141943511,2	MCF-7	breast:
18	chr3:23982130..23982921-chr3:141945206..141945893,2	MCF-7	breast:
19	chr3:141681155..141682217-chr3:141870930..141871455,3	MCF-7	breast:
20	chr3:141869138..141873341-chr3:141874948..141878227,4	MCF-7	breast:
21	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:
22	chr3:141920036..141922248-chr3:141942825..141944826,2	K562	blood:
23	chr3:141942954..141945885-chr3:141988032..141991755,3	MCF-7	breast:
24	chr3:141740878..141741732-chr3:141899625..141900228,2	MCF-7	breast:
25	chr3:141866424..141868170-chr3:141875148..141877149,2	MCF-7	breast:
26	chr1:45284275..45285951-chr3:141939370..141941710,2	K562	blood:
27	chr3:141456676..141459122-chr3:141866884..141869547,2	MCF-7	breast:
28	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
29	chr3:141866820..141869360-chr3:141877733..141879741,3	MCF-7	breast:
30	chr20:30192660..30193363-chr3:141943889..141944590,2	Hela-S3	cervix:
31	chr3:141924115..141926296-chr3:141927657..141929893,2	K562	blood:
32	chr3:141918898..141921887-chr3:141933656..141936243,2	K562	blood:
33	chr3:141884381..141887042-chr3:141942350..141944309,2	K562	blood:
34	chr3:141898603..141901511-chr3:141942977..141947111,4	MCF-7	breast:
35	chr3:141874750..141877739-chr3:141886968..141889204,2	K562	blood:
36	chr3:141745328..141748975-chr3:142003993..142005586,3	K562	blood:
37	chr3:141869138..141873341-chr3:141874948..141878227,4	MCF-7	breast:
38	chr3:141899683..141900200-chr3:141998508..141999054,2	K562	blood:
39	chr3:141944137..141946098-chr3:141949464..141952210,3	K562	blood:
40	chr3:141943457..141944964-chr3:141968920..141970444,2	MCF-7	breast:
41	chr3:141919674..141922479-chr3:141924056..141926779,2	MCF-7	breast:
42	chr3:141831489..141833335-chr3:141922195..141926170,3	K562	blood:
43	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
44	chr3:141899184..141899896-chr3:141998534..141999076,2	MCF-7	breast:
45	chr3:141872069..141873758-chr3:141878365..141880269,2	MCF-7	breast:
46	chr3:141998539..142000204-chr3:142002540..142004917,2	K562	blood:
47	chr3:141880531..141882859-chr3:141943394..141945714,2	K562	blood:
48	chr3:141940509..141943565-chr3:141944038..141945660,4	MCF-7	breast:
49	chr3:141983516..141986399-chr3:141987635..141990028,2	MCF-7	breast:
50	chr3:141918846..141920526-chr3:141922656..141925151,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TFDP2-7	chr3:141876369-141880820	ENSG00000272565.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	GK5	hsa-miR-340-5p	chr3:141878164-141878157
2	GK5	hsa-miR-124-3p	chr3:141883855-141883849

Variant related genes	Relation type
TFDP2	TF binding region
GK5	TF binding region
RNU6-425P	TF binding region
ENSG00000272565	TF binding region
TFDP2	CpG island
GK5	CpG island
RNU6-425P	CpG island
ENSG00000272565	CpG island
ENSG00000113387	chromatin interactions
ENSG00000175054	chromatin interactions
ENSG00000141526	chromatin interactions
ENSG00000122545	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000272565	chromatin interactions
ENSG00000114125	chromatin interactions
ENSG00000114126	chromatin interactions
ENSG00000130193	chromatin interactions
ENSG00000175066	chromatin interactions
ENSG00000266402	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000160183	chromatin interactions
ENSG00000253806	chromatin interactions
ENSG00000125968	chromatin interactions
ENSG00000199753	chromatin interactions
ENSG00000228878	chromatin interactions
ENSG00000206604	chromatin interactions
ENSG00000202444	chromatin interactions

Extended variants
information (count: 4994 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4994 , 50 per page) page: 1 2 3 4 5 6 7 ... 100

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6766782	chr3:141853926-141853927	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184413864	chr3:141853944-141853945	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs188711566	chr3:141853971-141853972	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79513925	chr3:141853976-141853977	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548677402	chr3:141853986-141853987	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370862372	chr3:141853997-141853998	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs139177261	chr3:141854014-141854015	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs534393457	chr3:141854032-141854033	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs73236032	chr3:141854074-141854075	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs571473811	chr3:141854101-141854102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs73236033	chr3:141854116-141854117	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs181195349	chr3:141854183-141854184	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs556668926	chr3:141854204-141854205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs575605748	chr3:141854205-141854206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs35321254	chr3:141854216-141854217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77066547	chr3:141854240-141854241	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542697844	chr3:141854315-141854316	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs541749016	chr3:141854323-141854324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs554997632	chr3:141854344-141854345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573401053	chr3:141854358-141854359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs540712654	chr3:141854363-141854364	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559600272	chr3:141854396-141854397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs532954624	chr3:141854419-141854420	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9757584	chr3:141854421-141854422	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs563395206	chr3:141854431-141854432	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373659894	chr3:141854497-141854498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11711563	chr3:141854506-141854507	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs11715702	chr3:141854515-141854516	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs11711629	chr3:141854524-141854525	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs11711565	chr3:141854527-141854528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs530822764	chr3:141854529-141854530	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11711632	chr3:141854537-141854538	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548598345	chr3:141854538-141854539	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11711633	chr3:141854544-141854545	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs11711569	chr3:141854545-141854546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566909309	chr3:141854571-141854572	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs199585570	chr3:141854596-141854597	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62284581	chr3:141854610-141854611	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs528189338	chr3:141854613-141854614	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs200829453	chr3:141854620-141854621	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs546261446	chr3:141854629-141854630	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185887125	chr3:141854658-141854659	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538819583	chr3:141854699-141854700	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557523925	chr3:141854706-141854707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs142308116	chr3:141854726-141854727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536927710	chr3:141854729-141854730	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555034544	chr3:141854739-141854740	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs377245143	chr3:141854816-141854817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs190348388	chr3:141854835-141854836	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs534306828	chr3:141854837-141854838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3056 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141836400-141866200	Weak transcription	Primary T cells from cord blood	blood
2	chr3:141838200-141866200	Weak transcription	Adipose Nuclei	Adipose
3	chr3:141840200-141865400	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:141840200-141866000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr3:141842800-141858400	Weak transcription	Fetal Intestine Large	intestine
6	chr3:141844800-141859600	Weak transcription	Fetal Stomach	stomach
7	chr3:141845000-141863600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:141845400-141867200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr3:141845600-141859000	Weak transcription	Thymus	Thymus
10	chr3:141847000-141859400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:141847400-141857800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr3:141847400-141859600	Weak transcription	Fetal Brain Female	brain
13	chr3:141848000-141866200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr3:141848200-141859000	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr3:141848200-141859600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr3:141848200-141859600	Weak transcription	Primary hematopoietic stem cells	blood
17	chr3:141848200-141866400	Weak transcription	Liver	Liver
18	chr3:141848400-141856400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
19	chr3:141849000-141866200	Weak transcription	Fetal Heart	heart
20	chr3:141849600-141859000	Weak transcription	Dnd41	blood
21	chr3:141850800-141859600	Weak transcription	Fetal Lung	lung
22	chr3:141851200-141866400	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr3:141853000-141854000	Enhancers	Brain Germinal Matrix	brain
24	chr3:141853000-141858400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr3:141853000-141859400	Weak transcription	Fetal Intestine Small	intestine
26	chr3:141853200-141855200	Strong transcription	Fetal Thymus	thymus
27	chr3:141853200-141859600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr3:141853800-141866200	Weak transcription	Brain Anterior Caudate	brain
29	chr3:141854000-141855800	Weak transcription	Brain Germinal Matrix	brain
30	chr3:141855200-141856400	Weak transcription	Fetal Thymus	thymus
31	chr3:141856000-141859000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr3:141856200-141863200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr3:141856400-141856600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr3:141856400-141856600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr3:141856400-141856600	ZNF genes & repeats	Brain Germinal Matrix	brain
36	chr3:141856400-141856800	Enhancers	K562	blood
37	chr3:141856400-141859400	Strong transcription	Fetal Thymus	thymus
38	chr3:141856600-141857800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:141856600-141859600	Weak transcription	Brain Germinal Matrix	brain
40	chr3:141856800-141859600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr3:141856800-141860000	Weak transcription	K562	blood
42	chr3:141857000-141858600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr3:141857200-141858800	Weak transcription	Duodenum Mucosa	Duodenum
44	chr3:141857200-141859600	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr3:141857600-141859600	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr3:141857600-141866400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr3:141857600-141867000	Weak transcription	Brain Substantia Nigra	brain
48	chr3:141857800-141858000	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:141857800-141859200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:141857800-141859600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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