Variant report

Variant	nsv877504
Chromosome Location	chr3:133122216-133172374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1012)
CpG islands
(count:366)
Chromatin interactive
region (count:52)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1012 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:133162975-133163294	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:133162962-133163067	K562	blood:	n/a	n/a
3	ARID3A	chr3:133156704-133157073	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:133171646-133172197	HepG2	liver:	n/a	n/a
5	ATF2	chr3:133167079-133168028	GM12878	blood:	n/a	n/a
6	ATF2	chr3:133142398-133142693	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr3:133166990-133168141	GM12878	blood:	n/a	n/a
8	ATF3	chr3:133162944-133163357	A549	lung:	n/a	n/a
9	BACH1	chr3:133163108-133163230	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:133163169-133163196	K562	blood:	n/a	n/a
11	BATF	chr3:133161396-133161659	GM12878	blood:	n/a	n/a
12	BATF	chr3:133167212-133168049	GM12878	blood:	n/a	n/a
13	BATF	chr3:133167292-133167760	GM12878	blood:	n/a	n/a
14	BATF	chr3:133168910-133169128	GM12878	blood:	n/a	n/a
15	BCL11A	chr3:133166638-133166892	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:133167273-133167755	GM12878	blood:	n/a	n/a
17	BCL11A	chr3:133167185-133167791	GM12878	blood:	n/a	n/a
18	BCL3	chr3:133162950-133163348	A549	lung:	n/a	n/a
19	BCL3	chr3:133167225-133167767	GM12878	blood:	n/a	n/a
20	BCL3	chr3:133162874-133163354	A549	lung:	n/a	n/a
21	BCLAF1	chr3:133167280-133167988	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:133160617-133161181	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:133167158-133167928	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:133144084-133144338	K562	blood:	n/a	chr3:133144178-133144199 chr3:133144184-133144193 chr3:133144183-133144192 chr3:133144184-133144193 chr3:133144182-133144195
25	BHLHE40	chr3:133143874-133144338	GM12878	blood:	n/a	chr3:133144178-133144199 chr3:133144184-133144193 chr3:133144183-133144192 chr3:133144184-133144193 chr3:133144182-133144195
26	BHLHE40	chr3:133144019-133144340	HepG2	liver:	n/a	chr3:133144178-133144199 chr3:133144184-133144193 chr3:133144183-133144192 chr3:133144184-133144193 chr3:133144182-133144195
27	BHLHE40	chr3:133160780-133160957	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:133166690-133168104	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:133142501-133142692	HepG2	liver:	n/a	n/a
30	BHLHE40	chr3:133132413-133132738	K562	blood:	n/a	n/a
31	CEBPB	chr3:133145164-133145977	IMR90	lung:	n/a	chr3:133145334-133145343 chr3:133145334-133145345
32	CEBPB	chr3:133159550-133159786	IMR90	lung:	n/a	n/a
33	CEBPB	chr3:133156748-133157253	A549	lung:	n/a	n/a
34	CEBPB	chr3:133145227-133145479	HepG2	liver:	n/a	chr3:133145334-133145343 chr3:133145334-133145345
35	CEBPB	chr3:133166948-133167249	HepG2	liver:	n/a	n/a
36	CEBPB	chr3:133162968-133163397	MCF-7	breast:	n/a	n/a
37	CEBPB	chr3:133167214-133168000	GM12878	blood:	n/a	n/a
38	CEBPB	chr3:133166852-133167302	MCF-7	breast:	n/a	n/a
39	CEBPB	chr3:133167344-133167767	GM12878	blood:	n/a	n/a
40	CEBPB	chr3:133170224-133170424	K562	blood:	n/a	n/a
41	CEBPB	chr3:133156900-133157098	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr3:133162967-133163321	A549	lung:	n/a	n/a
43	CEBPB	chr3:133156907-133157196	HepG2	liver:	n/a	n/a
44	CEBPB	chr3:133171735-133172159	A549	lung:	n/a	n/a
45	CEBPB	chr3:133156962-133157088	HepG2	liver:	n/a	n/a
46	CEBPB	chr3:133156923-133157154	A549	lung:	n/a	n/a
47	CEBPB	chr3:133142431-133142732	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr3:133166836-133167306	ECC-1	luminal epithelium:	n/a	n/a
49	CEBPB	chr3:133156910-133157182	A549	lung:	n/a	n/a
50	CEBPB	chr3:133156859-133157194	IMR90	lung:	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	chr3:133142442-133142492	H1-hESC	embryonic stem cell:	embryo
2	chr3:133131484-133131534	AG09319	gingival:	n/a
3	chr3:133129182-133129232	AG04449	skin:	fetal
4	chr3:133142442-133142492	SK-N-MC	brain:	n/a
5	chr3:133142442-133142492	AG04450	lung:	fetal
6	chr3:133129528-133129578	BE2_C	brain:	n/a
7	chr3:133123374-133123424	HNPCEpiC	eye:	n/a
8	chr3:133129182-133129232	GM19239	blood:	n/a
9	chr3:133142442-133142492	GM12891	blood:	n/a
10	chr3:133123374-133123424	HCPEpiC	choroid plexus:	n/a
11	chr3:133131484-133131534	NT2-D1	testis:	n/a
12	chr3:133129182-133129232	NHBE	bronchial:	n/a
13	chr3:133129528-133129578	HCT-116	colon:	n/a
14	chr3:133131484-133131534	IMR90	lung:	fetal
15	chr3:133160722-133160772	H1-hESC	embryonic stem cell:	embryo
16	chr3:133131484-133131534	A549	lung:	n/a
17	chr3:133123374-133123424	HRCEpiC	kidney:	n/a
18	chr3:133129182-133129232	HCPEpiC	choroid plexus:	n/a
19	chr3:133142442-133142492	HUVEC	blood vessel:	n/a
20	chr3:133129182-133129232	GM12878	blood:	n/a
21	chr3:133131484-133131534	GM19239	blood:	n/a
22	chr3:133123374-133123424	HAEpiC	amniotic membrane:	n/a
23	chr3:133129528-133129578	HRCEpiC	kidney:	n/a
24	chr3:133129528-133129578	Caco-2	colon:	n/a
25	chr3:133160722-133160772	AG09319	gingival:	n/a
26	chr3:133129182-133129232	RPTEC	kidney:	n/a
27	chr3:133131484-133131534	HRE	kidney:	n/a
28	chr3:133142442-133142492	HNPCEpiC	eye:	n/a
29	chr3:133131484-133131534	H1-hESC	embryonic stem cell:	embryo
30	chr3:133129528-133129578	HCPEpiC	choroid plexus:	n/a
31	chr3:133129528-133129578	AG04449	skin:	fetal
32	chr3:133129182-133129232	H1-hESC	embryonic stem cell:	embryo
33	chr3:133129528-133129578	GM12892	blood:	n/a
34	chr3:133160722-133160772	HMEC	breast:	n/a
35	chr3:133129182-133129232	HEEpiC	esophagus:	n/a
36	chr3:133123374-133123424	K562	blood:	n/a
37	chr3:133123374-133123424	SAEC	small airway:	n/a
38	chr3:133129182-133129232	ProgFib	skin:	n/a
39	chr3:133131484-133131534	MCF10A-Er-Src	breast:	n/a
40	chr3:133129528-133129578	HIPEpiC	eye:	n/a
41	chr3:133129182-133129232	HNPCEpiC	eye:	n/a
42	chr3:133142442-133142492	HMEC	breast:	n/a
43	chr3:133123374-133123424	HRE	kidney:	n/a
44	chr3:133160722-133160772	NHDF-neo	bronchial:	n/a
45	chr3:133160722-133160772	GM12891	blood:	n/a
46	chr3:133129528-133129578	NH-A	brain:	n/a
47	chr3:133123374-133123424	AG09319	gingival:	n/a
48	chr3:133129182-133129232	AG09319	gingival:	n/a
49	chr3:133131484-133131534	SAEC	small airway:	n/a
50	chr3:133131484-133131534	AG04450	lung:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr3:133130542..133132514-chr3:133135726..133138397,2	K562	blood:
2	chr3:133127092..133128594-chr3:133130623..133133431,2	K562	blood:
3	chr3:133127092..133128594-chr3:133130623..133133431,2	K562	blood:
4	chr3:133170213..133174135-chr3:133291301..133294544,7	MCF-7	breast:
5	chr3:133165936..133167701-chr3:133170915..133173583,2	MCF-7	breast:
6	chr3:9757483..9758292-chr3:133142110..133142638,2	MCF-7	breast:
7	chr3:132254793..132255497-chr3:133142223..133143012,2	MCF-7	breast:
8	chr3:133162655..133165073-chr3:133302328..133304905,2	MCF-7	breast:
9	chr3:133167229..133167755-chr3:133175434..133175991,2	MCF-7	breast:
10	chr3:133153374..133155623-chr3:133178756..133181568,2	MCF-7	breast:
11	chr3:133162344..133164568-chr3:133170486..133172340,2	MCF-7	breast:
12	chr3:133103700..133105206-chr3:133145260..133147537,2	MCF-7	breast:
13	chr3:132759801..132760742-chr3:133142128..133143076,4	K562	blood:
14	chr3:133112630..133114708-chr3:133139610..133142045,2	MCF-7	breast:
15	chr3:133103081..133103646-chr3:133142086..133142975,2	MCF-7	breast:
16	chr3:133161126..133163362-chr3:133716874..133718991,2	MCF-7	breast:
17	chr3:133116761..133118281-chr3:133121220..133123369,2	MCF-7	breast:
18	chr3:133161498..133163430-chr3:133177580..133180492,2	MCF-7	breast:
19	chr3:132450041..132450545-chr3:133142532..133143079,2	MCF-7	breast:
20	chr3:133157614..133159681-chr3:133160592..133163349,2	MCF-7	breast:
21	chr3:132445024..132445748-chr3:133142162..133143068,3	MCF-7	breast:
22	chr3:132444895..132445778-chr3:133142129..133143849,5	K562	blood:
23	chr3:132443404..132445988-chr3:133125614..133127978,2	MCF-7	breast:
24	chr3:133169681..133172224-chr3:133173356..133176269,2	K562	blood:
25	chr3:133162011..133163962-chr3:133171581..133174008,3	MCF-7	breast:
26	chr3:133157939..133159842-chr3:133161653..133163728,2	MCF-7	breast:
27	chr3:133164640..133168534-chr3:133291750..133294077,5	MCF-7	breast:
28	chr3:133169398..133190840-chr3:133288286..133298861,41	MCF-7	breast:
29	chr3:133162579..133164484-chr3:133291508..133294173,3	MCF-7	breast:
30	chr3:133157614..133159681-chr3:133160592..133163349,2	MCF-7	breast:
31	chr3:133105226..133106115-chr3:133142183..133142702,2	MCF-7	breast:
32	chr3:133155512..133157833-chr3:133291235..133293507,2	MCF-7	breast:
33	chr3:132759782..132760302-chr3:133142211..133142884,2	MCF-7	breast:
34	chr3:133162011..133163962-chr3:133171581..133174008,3	MCF-7	breast:
35	chr3:133130542..133132514-chr3:133135726..133138397,2	K562	blood:
36	chr3:132450051..132450561-chr3:133142135..133143010,2	MCF-7	breast:
37	chr3:132759750..132760749-chr3:133142099..133143085,7	MCF-7	breast:
38	chr3:133105415..133106537-chr3:133142074..133142947,6	MCF-7	breast:
39	chr3:133165936..133167701-chr3:133170915..133173583,2	MCF-7	breast:
40	chr3:133159700..133161367-chr3:133523361..133526240,2	MCF-7	breast:
41	chr3:133162344..133164568-chr3:133170486..133172340,2	MCF-7	breast:
42	chr3:133155354..133158074-chr3:133292278..133293875,2	MCF-7	breast:
43	chr3:132449765..132450613-chr3:133142265..133142889,2	K562	blood:
44	chr3:132440764..132443232-chr3:133142306..133144547,2	MCF-7	breast:
45	chr3:133146085..133148197-chr3:133291906..133294267,2	MCF-7	breast:
46	chr3:133162782..133163438-chr3:133297156..133297900,2	MCF-7	breast:
47	chr3:133143999..133146404-chr3:133171252..133173491,2	MCF-7	breast:
48	chr3:133157939..133159842-chr3:133161653..133163728,2	MCF-7	breast:
49	chr3:132439632..132442220-chr3:133141166..133143810,2	K562	blood:
50	chr3:133170643..133173658-chr3:133173707..133177209,4	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOPBP1-1	chr3:133148113-133148553	ENSG00000249993.1
2	lnc-TOPBP1-1	chr3:133164249-133164419	ENSG00000249993.1
3	lnc-TMEM108-2	chr3:133128799-133129687	NONHSAT092184
4	lnc-TOPBP1-1	chr3:133167625-133167739	ENSG00000249993.1
5	lnc-TOPBP1-6	chr3:133131577-133131725	NONHSAT092182

No data

Variant related genes	Relation type
ENSG00000249820	TF binding region
BFSP2	TF binding region
ENSG00000249820	CpG island
BFSP2	CpG island
ENSG00000091527	chromatin interactions
ENSG00000249993	chromatin interactions
ENSG00000248724	chromatin interactions
ENSG00000144868	chromatin interactions
ENSG00000113971	chromatin interactions
ENSG00000144867	chromatin interactions

Extended variants
information (count: 2167 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:2167 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1842156	chr3:133122216-133122217	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147899043	chr3:133122230-133122231	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs71317406	chr3:133122237-133122238	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs549895582	chr3:133122282-133122283	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs112381495	chr3:133122285-133122286	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs562583005	chr3:133122348-133122349	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs532210318	chr3:133122410-133122411	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs551969995	chr3:133122411-133122412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs188914334	chr3:133122436-133122437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1513360	chr3:133122468-133122469	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534613118	chr3:133122478-133122479	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs193068592	chr3:133122535-133122536	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs568486777	chr3:133122552-133122553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537125293	chr3:133122553-133122554	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557460675	chr3:133122561-133122562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs618971	chr3:133122629-133122630	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs79962396	chr3:133122729-133122730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553610114	chr3:133122805-133122806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs573540140	chr3:133122827-133122828	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs542588032	chr3:133122828-133122829	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78968293	chr3:133122843-133122844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565446396	chr3:133122927-133122928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs78236836	chr3:133122930-133122931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs574403236	chr3:133122945-133122946	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs146982917	chr3:133122957-133122958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs372091096	chr3:133123234-133123235	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs563363610	chr3:133123263-133123264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73863529	chr3:133123287-133123288	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs185798561	chr3:133123296-133123297	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs559162641	chr3:133123318-133123319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368459668	chr3:133123355-133123356	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs147602736	chr3:133123360-133123361	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548489071	chr3:133123416-133123417	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568344618	chr3:133123419-133123420	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537415771	chr3:133123424-133123425	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547693048	chr3:133123434-133123435	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs550719763	chr3:133123455-133123456	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs570914025	chr3:133123557-133123558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs539951208	chr3:133123560-133123561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs35119880	chr3:133123589-133123590	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553597861	chr3:133123591-133123592	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs140835358	chr3:133123613-133123614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535751932	chr3:133123645-133123646	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567345001	chr3:133123650-133123651	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs556060823	chr3:133123678-133123679	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs116517915	chr3:133123686-133123687	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs543379912	chr3:133123689-133123690	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563145514	chr3:133123691-133123692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1153876	chr3:133123736-133123737	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs545541266	chr3:133123839-133123840	Enhancers Weak transcription	TF binding region	1 gene(s)	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
Cancer	21129771	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
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	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
Hailey-hailey disease	17597066	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
small cell lung cancer	20016488	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:666 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133099600-133122600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr3:133103400-133123200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr3:133103400-133123600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr3:133103800-133123800	Weak transcription	Brain Anterior Caudate	brain
5	chr3:133104400-133131400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr3:133107200-133123800	Weak transcription	Fetal Thymus	thymus
7	chr3:133110800-133123600	Weak transcription	HSMM	muscle
8	chr3:133113600-133123600	Weak transcription	HSMMtube	muscle
9	chr3:133114200-133127400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:133120800-133123600	Weak transcription	Fetal Brain Female	brain
11	chr3:133121000-133123600	Weak transcription	Brain Germinal Matrix	brain
12	chr3:133121200-133122600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr3:133121600-133124800	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr3:133121800-133122800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr3:133122000-133122400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
16	chr3:133122000-133124000	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr3:133122000-133124200	Enhancers	Brain Hippocampus Middle	brain
18	chr3:133122000-133124600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr3:133122200-133122800	Enhancers	Fetal Lung	lung
20	chr3:133122200-133123000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr3:133122200-133123000	Enhancers	Brain Angular Gyrus	brain
22	chr3:133122200-133123800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr3:133122200-133124000	Enhancers	Brain Substantia Nigra	brain
24	chr3:133122200-133124000	Enhancers	Fetal Muscle Leg	muscle
25	chr3:133122200-133124200	Enhancers	Brain Cingulate Gyrus	brain
26	chr3:133122200-133124200	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr3:133122400-133124000	Enhancers	Fetal Muscle Trunk	muscle
28	chr3:133122600-133123600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
29	chr3:133122600-133124400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr3:133122800-133128000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr3:133122800-133129400	Weak transcription	Fetal Lung	lung
32	chr3:133123000-133123800	Weak transcription	Brain Angular Gyrus	brain
33	chr3:133123000-133131800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr3:133123200-133124000	Enhancers	H1 Cell Line	embryonic stem cell
35	chr3:133123400-133124400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:133123600-133123800	Enhancers	H9 Cell Line	embryonic stem cell
37	chr3:133123600-133124000	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr3:133123600-133124000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
39	chr3:133123600-133124200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr3:133123600-133124200	Enhancers	Fetal Brain Female	brain
41	chr3:133123600-133124200	Enhancers	HSMM	muscle
42	chr3:133123600-133124400	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:133123600-133124400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr3:133123600-133124400	Enhancers	Brain Germinal Matrix	brain
45	chr3:133123600-133124400	Enhancers	HSMMtube	muscle
46	chr3:133123800-133124000	Enhancers	Brain Angular Gyrus	brain
47	chr3:133123800-133124000	Enhancers	Brain Anterior Caudate	brain
48	chr3:133123800-133124200	Enhancers	Fetal Thymus	thymus
49	chr3:133123800-133131400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr3:133124000-133124400	Enhancers	ES-I3 Cell Line	embryonic stem cell

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