Variant report

Variant	esv2753915
Chromosome Location	chr3:85071410-85624810
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:85616263-85616538	K562	blood:	n/a	n/a
2	ARID3A	chr3:85139849-85139961	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:85552489-85553162	K562	blood:	n/a	chr3:85552542-85552558
4	ARID3A	chr3:85553514-85553826	K562	blood:	n/a	n/a
5	ARID3A	chr3:85609707-85609851	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:85210694-85210953	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:85554724-85556040	K562	blood:	n/a	chr3:85555983-85555999 chr3:85555685-85555701
8	BACH1	chr3:85212144-85212205	K562	blood:	n/a	n/a
9	BACH1	chr3:85531095-85531395	K562	blood:	n/a	n/a
10	BACH1	chr3:85556142-85556514	K562	blood:	n/a	n/a
11	BACH1	chr3:85501073-85501146	K562	blood:	n/a	n/a
12	BACH1	chr3:85212123-85212403	H1-hESC	embryonic stem cell:	n/a	chr3:85212215-85212229
13	BCLAF1	chr3:85552292-85553331	K562	blood:	n/a	n/a
14	BHLHE40	chr3:85616320-85616579	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:85553505-85553787	K562	blood:	n/a	n/a
16	BHLHE40	chr3:85208583-85208600	A549	lung:	n/a	n/a
17	BRCA1	chr3:85130364-85131104	Hela-S3	cervix:	n/a	n/a
18	CBX3	chr3:85553411-85553733	K562	blood:	n/a	n/a
19	CCNT2	chr3:85553578-85553965	K562	blood:	n/a	n/a
20	CEBPB	chr3:85235859-85235971	A549	lung:	n/a	chr3:85235911-85235922
21	CEBPB	chr3:85496661-85496884	A549	lung:	n/a	n/a
22	CEBPB	chr3:85544048-85544400	K562	blood:	n/a	chr3:85544227-85544236 chr3:85544226-85544237 chr3:85544227-85544236 chr3:85544225-85544238 chr3:85544227-85544236
23	CEBPB	chr3:85101099-85101299	H1-hESC	embryonic stem cell:	n/a	chr3:85101167-85101178
24	CEBPB	chr3:85609588-85609927	HepG2	liver:	n/a	chr3:85609764-85609775 chr3:85609765-85609776 chr3:85609764-85609777
25	CEBPB	chr3:85144871-85145071	H1-hESC	embryonic stem cell:	n/a	chr3:85145027-85145036 chr3:85145025-85145036
26	CEBPB	chr3:85106821-85107009	A549	lung:	n/a	chr3:85106916-85106927 chr3:85106918-85106927 chr3:85106918-85106929
27	CEBPB	chr3:85583536-85583843	IMR90	lung:	n/a	chr3:85583673-85583684
28	CEBPB	chr3:85130354-85130780	A549	lung:	n/a	chr3:85130589-85130601
29	CEBPB	chr3:85267404-85267669	A549	lung:	n/a	chr3:85267508-85267519 chr3:85267507-85267520
30	CEBPB	chr3:85320100-85320366	MCF-7	breast:	n/a	n/a
31	CEBPB	chr3:85232926-85233143	HepG2	liver:	n/a	chr3:85232999-85233010
32	CEBPB	chr3:85106812-85107011	H1-hESC	embryonic stem cell:	n/a	chr3:85106916-85106927 chr3:85106918-85106927 chr3:85106918-85106929
33	CEBPB	chr3:85208212-85208478	H1-hESC	embryonic stem cell:	n/a	chr3:85208316-85208327
34	CEBPB	chr3:85106817-85107091	HepG2	liver:	n/a	chr3:85106916-85106927 chr3:85106918-85106927 chr3:85106918-85106929
35	CEBPB	chr3:85583548-85583816	A549	lung:	n/a	chr3:85583673-85583684
36	CEBPB	chr3:85511812-85512152	HepG2	liver:	n/a	chr3:85511970-85511983 chr3:85511970-85511981 chr3:85511970-85511983 chr3:85511972-85511983
37	CEBPB	chr3:85509318-85509320	A549	lung:	n/a	n/a
38	CEBPB	chr3:85551299-85551609	K562	blood:	n/a	chr3:85551467-85551480 chr3:85551469-85551480
39	CEBPB	chr3:85210692-85211043	A549	lung:	n/a	n/a
40	CEBPB	chr3:85423175-85423346	H1-hESC	embryonic stem cell:	n/a	chr3:85423236-85423247
41	CEBPB	chr3:85478280-85478610	A549	lung:	n/a	chr3:85478503-85478516 chr3:85478503-85478514 chr3:85478426-85478437
42	CEBPB	chr3:85509356-85509533	HepG2	liver:	n/a	chr3:85509405-85509418 chr3:85509406-85509417
43	CEBPB	chr3:85547527-85547844	HepG2	liver:	n/a	chr3:85547688-85547701 chr3:85547688-85547699
44	CEBPB	chr3:85222681-85223019	IMR90	lung:	n/a	chr3:85222841-85222852 chr3:85222840-85222853
45	CEBPB	chr3:85423130-85423398	A549	lung:	n/a	chr3:85423236-85423247
46	CEBPB	chr3:85440604-85440910	HepG2	liver:	n/a	chr3:85440748-85440759 chr3:85440750-85440759 chr3:85440748-85440761 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440750-85440759 chr3:85440749-85440760 chr3:85440748-85440761
47	CEBPB	chr3:85533186-85533637	K562	blood:	n/a	n/a
48	CEBPB	chr3:85208203-85208493	A549	lung:	n/a	chr3:85208316-85208327
49	CEBPB	chr3:85086253-85086378	H1-hESC	embryonic stem cell:	n/a	chr3:85086271-85086282
50	CEBPB	chr3:85544047-85544392	IMR90	lung:	n/a	chr3:85544227-85544236 chr3:85544226-85544237 chr3:85544227-85544236 chr3:85544225-85544238 chr3:85544227-85544236

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:85071786-85071836	AG04449	skin:	fetal
2	chr3:85213671-85213721	SAEC	small airway:	n/a
3	chr3:85071786-85071836	AG04449	skin:	fetal
4	chr3:85213671-85213721	SAEC	small airway:	n/a
5	chr3:85178247-85178297	LNCaP	prostate:	n/a
6	chr3:85544609-85544659	HPAEpiC	pulmonary alveolar:	n/a
7	chr3:85079961-85080011	T-47D	breast:	n/a
8	chr3:85213671-85213721	RPTEC	kidney:	n/a
9	chr3:85213671-85213721	GM19239	blood:	n/a
10	chr3:85213671-85213721	SK-N-MC	brain:	n/a
11	chr3:85071786-85071836	GM12891	blood:	n/a
12	chr3:85512134-85512184	SKMC	muscle:	n/a
13	chr3:85213671-85213721	AG04449	skin:	fetal
14	chr3:85178247-85178297	HUVEC	blood vessel:	n/a
15	chr3:85512134-85512184	HepG2	liver:	n/a
16	chr3:85512134-85512184	HPAEpiC	pulmonary alveolar:	n/a
17	chr3:85140079-85140129	HEEpiC	esophagus:	n/a
18	chr3:85512134-85512184	SK-N-SH	brain:	n/a
19	chr3:85140079-85140129	ovcar-3	ovarian:	n/a
20	chr3:85178247-85178297	Hela-S3	cervix:	n/a
21	chr3:85512134-85512184	GM19239	blood:	n/a
22	chr3:85544609-85544659	HRCEpiC	kidney:	n/a
23	chr3:85512134-85512184	MCF-7	breast:	n/a
24	chr3:85071786-85071836	HL-60	blood:	n/a
25	chr3:85071786-85071836	K562	blood:	n/a
26	chr3:85512134-85512184	U87	brain:	n/a
27	chr3:85553266-85553316	SAEC	small airway:	n/a
28	chr3:85512134-85512184	AG04449	skin:	fetal
29	chr3:85071786-85071836	HIPEpiC	eye:	n/a
30	chr3:85544609-85544659	NB4	blood:	n/a
31	chr3:85213671-85213721	HEEpiC	esophagus:	n/a
32	chr3:85140079-85140129	Jurkat	blood:	n/a
33	chr3:85213671-85213721	A549	lung:	n/a
34	chr3:85213671-85213721	SKMC	muscle:	n/a
35	chr3:85213671-85213721	HRE	kidney:	n/a
36	chr3:85140079-85140129	PrEC	prostate:	n/a
37	chr3:85213671-85213721	ovcar-3	ovarian:	n/a
38	chr3:85178247-85178297	HEEpiC	esophagus:	n/a
39	chr3:85544609-85544659	NHDF-neo	bronchial:	n/a
40	chr3:85079961-85080011	H1-hESC	embryonic stem cell:	embryo
41	chr3:85553266-85553316	SK-N-SH_RA	brain:	n/a
42	chr3:85544609-85544659	HEEpiC	esophagus:	n/a
43	chr3:85544609-85544659	AG09309	skin:	n/a
44	chr3:85544609-85544659	AG09319	gingival:	n/a
45	chr3:85140079-85140129	SAEC	small airway:	n/a
46	chr3:85071786-85071836	MCF10A-Er-Src	breast:	n/a
47	chr3:85544609-85544659	AG10803	skin:	n/a
48	chr3:85213671-85213721	HCT-116	colon:	n/a
49	chr3:85079961-85080011	HepG2	liver:	n/a
50	chr3:85071786-85071836	ovcar-3	ovarian:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:85503835..85505718-chr3:85553016..85554877,3	K562	blood:
2	chr3:85582405..85584379-chr3:85589105..85591498,2	K562	blood:
3	chr3:84291765..84296920-chr3:85550637..85554814,6	K562	blood:
4	chr3:85489023..85491028-chr3:85614972..85617090,2	K562	blood:
5	chr3:85554458..85559025-chr3:85559659..85564098,6	K562	blood:
6	chr3:85509846..85512397-chr3:85550866..85553089,2	K562	blood:
7	chr3:84609476..84611998-chr3:85551707..85553249,2	K562	blood:
8	chr3:85569919..85571559-chr3:85571800..85574471,2	K562	blood:
9	chr3:85353291..85354669-chr3:85409554..85410988,3	K562	blood:
10	chr3:85455981..85458898-chr3:85554544..85556051,2	K562	blood:
11	chr3:85550694..85553715-chr3:85562655..85565189,4	K562	blood:
12	chr3:85425596..85428443-chr3:85428590..85430282,2	K562	blood:
13	chr14:33567272..33568194-chr3:85240415..85241255,2	MCF-7	breast:
14	chr3:85516644..85518723-chr3:85527589..85529747,2	K562	blood:
15	chr3:85453248..85455514-chr3:85462247..85464334,2	K562	blood:
16	chr3:85550694..85553715-chr3:85562655..85565189,4	K562	blood:
17	chr3:85353497..85354172-chr3:85624891..85625399,2	MCF-7	breast:
18	chr3:84597130..84597691-chr3:85409635..85410581,3	MCF-7	breast:
19	chr3:85353629..85354290-chr3:85624959..85625479,2	K562	blood:
20	chr3:85353254..85353869-chr3:85625261..85626043,2	MCF-7	breast:
21	chr3:85522620..85526472-chr3:85527505..85529886,4	K562	blood:
22	chr3:85487121..85488806-chr3:85536380..85538383,2	K562	blood:
23	chr3:85468729..85471491-chr3:85479728..85483045,3	K562	blood:
24	chr3:85023240..85023756-chr3:85409642..85410352,2	MCF-7	breast:
25	chr3:85520722..85524381-chr3:85549502..85554850,5	K562	blood:
26	chr3:85091072..85092895-chr3:85093228..85096203,2	K562	blood:
27	chr2:75010074..75010799-chr3:85210133..85210807,2	MCF-7	breast:
28	chr3:85551480..85554348-chr3:85623401..85624978,2	K562	blood:
29	chr3:85512384..85516287-chr3:85548853..85551591,3	K562	blood:
30	chr3:85453248..85455514-chr3:85462247..85464334,2	K562	blood:
31	chr3:85510863..85513429-chr3:85513950..85516943,2	MCF-7	breast:
32	chr3:85461933..85464830-chr3:85550203..85551783,2	K562	blood:
33	chr3:85486960..85489003-chr3:85551718..85553697,2	K562	blood:
34	chr3:85503835..85505718-chr3:85553016..85554877,3	K562	blood:
35	chr3:85513919..85516830-chr3:85552866..85555627,2	K562	blood:
36	chr3:84994697..84996927-chr3:85551100..85552839,2	K562	blood:
37	chr3:85510932..85513927-chr3:85533761..85535530,2	K562	blood:
38	chr3:85353354..85354461-chr3:85391496..85392792,4	MCF-7	breast:
39	chr3:85518552..85520271-chr3:85524775..85526982,3	K562	blood:
40	chr3:85243785..85244488-chr6:122933006..122933585,2	MCF-7	breast:
41	chr3:85550792..85552939-chr3:85620775..85622757,2	K562	blood:
42	chr3:85448906..85450732-chr3:85454290..85457141,2	K562	blood:
43	chr3:85528291..85540418-chr3:85548148..85554862,16	K562	blood:
44	chr3:85534090..85536047-chr3:85539153..85540993,2	K562	blood:
45	chr3:85277464..85279349-chr3:85282954..85285645,2	MCF-7	breast:
46	chr3:85476815..85480076-chr3:85489792..85493283,3	K562	blood:
47	chr3:85425596..85428443-chr3:85428590..85430282,2	K562	blood:
48	chr3:85554458..85559025-chr3:85559659..85564098,6	K562	blood:
49	chr3:85439579..85441215-chr3:85551442..85553756,2	K562	blood:
50	chr3:85353291..85354669-chr3:85409554..85410988,3	K562	blood:

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5688	chr3:85434911-85434932	MIMAT0022479

Variant related genes	Relation type
MIR5688	TF binding region
MIR5688	CpG island
ENSG00000212195	chromatin interactions

Extended variants
information (count: 15144 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:15144 , 50 per page) page: 1 2 3 4 5 6 7 ... 303

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs41363247	chr3:85071447-85071448	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs543058971	chr3:85071488-85071489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs765464	chr3:85071538-85071539	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs765463	chr3:85071549-85071550	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573314577	chr3:85071554-85071555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544378834	chr3:85071556-85071557	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs765462	chr3:85071568-85071569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs41425244	chr3:85071585-85071586	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs185150742	chr3:85071627-85071628	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs765461	chr3:85071640-85071641	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs544502623	chr3:85071666-85071667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs563051959	chr3:85071676-85071677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs530531165	chr3:85071728-85071729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146609875	chr3:85071786-85071787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs139841133	chr3:85071787-85071788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs528104391	chr3:85071811-85071812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs546174706	chr3:85071817-85071818	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs571222156	chr3:85071926-85071927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs76773157	chr3:85071994-85071995	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556878011	chr3:85072016-85072017	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs568990768	chr3:85072039-85072040	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs575604740	chr3:85072061-85072062	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs12633800	chr3:85072070-85072071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536048985	chr3:85072110-85072111	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149698602	chr3:85072193-85072194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs573351723	chr3:85072297-85072298	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540663724	chr3:85072298-85072299	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73139687	chr3:85072308-85072309	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs201812745	chr3:85072325-85072326	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs577473168	chr3:85072329-85072330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111689040	chr3:85072363-85072364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs544850060	chr3:85072395-85072396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs560544442	chr3:85072445-85072446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs189921243	chr3:85072454-85072455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532524374	chr3:85072492-85072493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542000304	chr3:85072503-85072504	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs2200472	chr3:85072584-85072585	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs576237725	chr3:85072599-85072600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs528142544	chr3:85072628-85072629	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182004818	chr3:85072677-85072678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571173258	chr3:85072695-85072696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs73139689	chr3:85072698-85072699	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs538082143	chr3:85072732-85072733	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550891414	chr3:85072775-85072776	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs145452501	chr3:85072807-85072808	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377551115	chr3:85072818-85072819	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536478166	chr3:85072862-85072863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs201262733	chr3:85072924-85072925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs548389090	chr3:85072932-85072933	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566993393	chr3:85073029-85073030	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Mental retardation	17124404	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Autism	22102821	CNVD
Prostate cancer	21307934	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1045 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:85055800-85081400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr3:85065200-85082200	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:85068600-85090600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr3:85070000-85073000	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr3:85070600-85072800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr3:85070600-85073000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr3:85071000-85073400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr3:85071200-85071600	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr3:85071200-85071600	Enhancers	Brain Substantia Nigra	brain
10	chr3:85071200-85071800	Enhancers	Brain Angular Gyrus	brain
11	chr3:85071400-85071600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
12	chr3:85071400-85071800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:85071400-85071800	Enhancers	Brain Anterior Caudate	brain
14	chr3:85071400-85071800	Enhancers	Brain Inferior Temporal Lobe	brain
15	chr3:85071400-85082400	Weak transcription	Fetal Brain Female	brain
16	chr3:85071600-85071800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr3:85071600-85073000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr3:85071600-85074400	Weak transcription	Brain Substantia Nigra	brain
19	chr3:85071600-85082000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
20	chr3:85071800-85072800	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr3:85071800-85073000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr3:85071800-85081400	Weak transcription	Brain Angular Gyrus	brain
23	chr3:85072800-85073600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr3:85072800-85073800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr3:85073000-85073200	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr3:85073000-85073600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr3:85073000-85073600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:85073000-85074000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr3:85073200-85073600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr3:85073400-85077200	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr3:85073600-85078400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
32	chr3:85073600-85078600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr3:85073600-85078800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
34	chr3:85073600-85079000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr3:85073800-85078400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr3:85074000-85079000	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr3:85074400-85075000	Enhancers	Brain Substantia Nigra	brain
38	chr3:85077200-85077800	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr3:85077800-85078200	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr3:85078200-85080400	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:85078400-85079000	Enhancers	iPS-20b Cell Line	embryonic stem cell
42	chr3:85078400-85080000	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr3:85078600-85078800	Enhancers	Brain Inferior Temporal Lobe	brain
44	chr3:85078600-85079000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
45	chr3:85078600-85080000	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr3:85078800-85079600	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr3:85078800-85081800	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr3:85079000-85079600	Enhancers	H9 Cell Line	embryonic stem cell
49	chr3:85079000-85079600	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr3:85079000-85079600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell

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