Variant report

Variant	nsv1052492
Chromosome Location	chr9:104263419-104387782
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1708)
CpG islands
(count:671)
Chromatin interactive
region (count:45)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1708 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:104333522-104333644	K562	blood:	n/a	n/a
2	ARID3A	chr9:104295942-104296283	K562	blood:	n/a	n/a
3	ARID3A	chr9:104292514-104292714	HepG2	liver:	n/a	n/a
4	ATF1	chr9:104295646-104296267	K562	blood:	n/a	n/a
5	ATF2	chr9:104292374-104292716	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr9:104292401-104292766	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr9:104364431-104364849	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr9:104344911-104345228	K562	blood:	n/a	n/a
9	BACH1	chr9:104296093-104296404	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr9:104286436-104286549	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr9:104365147-104365162	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr9:104348916-104349355	GM12878	blood:	n/a	chr9:104349134-104349144 chr9:104349138-104349148 chr9:104349137-104349148
13	BATF	chr9:104348957-104349325	GM12878	blood:	n/a	chr9:104349134-104349144 chr9:104349138-104349148 chr9:104349137-104349148
14	BATF	chr9:104381008-104381267	GM12878	blood:	n/a	n/a
15	BATF	chr9:104273117-104273328	GM12878	blood:	n/a	chr9:104273227-104273238
16	BATF	chr9:104311800-104312003	GM12878	blood:	n/a	n/a
17	BATF	chr9:104380995-104381316	GM12878	blood:	n/a	n/a
18	BATF	chr9:104329547-104329786	GM12878	blood:	n/a	n/a
19	BATF	chr9:104329511-104329874	GM12878	blood:	n/a	n/a
20	BCL11A	chr9:104349027-104349291	GM12878	blood:	n/a	chr9:104349137-104349146 chr9:104349136-104349145
21	BCL3	chr9:104385443-104385668	GM12878	blood:	n/a	chr9:104385479-104385488
22	BCLAF1	chr9:104292317-104292714	GM12878	blood:	n/a	n/a
23	BHLHE40	chr9:104295886-104296435	A549	lung:	n/a	n/a
24	BHLHE40	chr9:104292414-104292743	GM12878	blood:	n/a	n/a
25	BHLHE40	chr9:104295571-104296450	GM12878	blood:	n/a	n/a
26	BHLHE40	chr9:104299234-104299490	K562	blood:	n/a	n/a
27	BHLHE40	chr9:104295506-104296590	K562	blood:	n/a	n/a
28	BHLHE40	chr9:104295750-104296587	HepG2	liver:	n/a	n/a
29	BRCA1	chr9:104331744-104331753	HepG2	liver:	n/a	n/a
30	BRCA1	chr9:104295333-104296540	Hela-S3	cervix:	n/a	chr9:104295834-104295841
31	BRCA1	chr9:104276469-104276627	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr9:104296137-104296265	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr9:104364506-104364922	H1-hESC	embryonic stem cell:	n/a	n/a
34	BRCA1	chr9:104295927-104296269	HepG2	liver:	n/a	n/a
35	CBX3	chr9:104295495-104296375	K562	blood:	n/a	n/a
36	CCNT2	chr9:104369821-104369931	K562	blood:	n/a	n/a
37	CEBPB	chr9:104295753-104296739	HepG2	liver:	n/a	n/a
38	CEBPB	chr9:104274349-104274691	IMR90	lung:	n/a	n/a
39	CEBPB	chr9:104298679-104298980	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr9:104353213-104353473	K562	blood:	n/a	chr9:104353309-104353326
41	CEBPB	chr9:104270526-104270858	IMR90	lung:	n/a	n/a
42	CEBPB	chr9:104364439-104364786	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr9:104292355-104292675	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPB	chr9:104364515-104364796	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr9:104289419-104289723	IMR90	lung:	n/a	n/a
46	CEBPB	chr9:104364482-104364733	K562	blood:	n/a	n/a
47	CEBPB	chr9:104274383-104274760	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr9:104295668-104296208	K562	blood:	n/a	n/a
49	CEBPB	chr9:104277520-104277610	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr9:104295675-104296277	A549	lung:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:104334427-104334477	NHBE	bronchial:	n/a
2	chr9:104295276-104295326	HCPEpiC	choroid plexus:	n/a
3	chr9:104295632-104295682	Hela-S3	cervix:	n/a
4	chr9:104334427-104334477	K562	blood:	n/a
5	chr9:104356619-104356669	HepG2	liver:	n/a
6	chr9:104356619-104356669	ProgFib	skin:	n/a
7	chr9:104292242-104292292	NB4	blood:	n/a
8	chr9:104357967-104358017	GM06990	blood:	n/a
9	chr9:104305608-104305658	HIPEpiC	eye:	n/a
10	chr9:104356619-104356669	Hepatocyte	liver:	n/a
11	chr9:104292242-104292292	AG09319	gingival:	n/a
12	chr9:104295632-104295682	H1-hESC	embryonic stem cell:	embryo
13	chr9:104357967-104358017	NHBE	bronchial:	n/a
14	chr9:104357967-104358017	AoSMC	blood vessel:	n/a
15	chr9:104357967-104358017	A549	lung:	n/a
16	chr9:104357967-104358017	HCF	heart:	n/a
17	chr9:104305608-104305658	AG04449	skin:	fetal
18	chr9:104357177-104357227	HCF	heart:	n/a
19	chr9:104295632-104295682	HAEpiC	amniotic membrane:	n/a
20	chr9:104294981-104295031	SK-N-MC	brain:	n/a
21	chr9:104292242-104292292	AG09309	skin:	n/a
22	chr9:104296226-104296276	HMEC	breast:	n/a
23	chr9:104294981-104295031	T-47D	breast:	n/a
24	chr9:104294981-104295031	MCF-7	breast:	n/a
25	chr9:104296226-104296276	ECC-1	luminal epithelium:	n/a
26	chr9:104357967-104358017	AG10803	skin:	n/a
27	chr9:104292242-104292292	Jurkat	blood:	n/a
28	chr9:104295276-104295326	SKMC	muscle:	n/a
29	chr9:104357177-104357227	SK-N-MC	brain:	n/a
30	chr9:104294981-104295031	H1-hESC	embryonic stem cell:	embryo
31	chr9:104294981-104295031	Hepatocyte	liver:	n/a
32	chr9:104358101-104358151	IMR90	lung:	fetal
33	chr9:104357967-104358017	GM12892	blood:	n/a
34	chr9:104294981-104295031	HPAEpiC	pulmonary alveolar:	n/a
35	chr9:104294981-104295031	GM12892	blood:	n/a
36	chr9:104292242-104292292	H1-hESC	embryonic stem cell:	embryo
37	chr9:104295632-104295682	AG09309	skin:	n/a
38	chr9:104357967-104358017	AG09309	skin:	n/a
39	chr9:104295276-104295326	AG09309	skin:	n/a
40	chr9:104295632-104295682	GM12892	blood:	n/a
41	chr9:104295632-104295682	AG04449	skin:	fetal
42	chr9:104357177-104357227	BE2_C	brain:	n/a
43	chr9:104294981-104295031	K562	blood:	n/a
44	chr9:104334427-104334477	GM06990	blood:	n/a
45	chr9:104296226-104296276	T-47D	breast:	n/a
46	chr9:104356619-104356669	GM12878	blood:	n/a
47	chr9:104358101-104358151	GM12878	blood:	n/a
48	chr9:104305608-104305658	BJ	skin:	n/a
49	chr9:104294981-104295031	HCPEpiC	choroid plexus:	n/a
50	chr9:104292242-104292292	K562	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:104369041..104371983-chr9:104372682..104374513,2	MCF-7	breast:
2	chr9:104210438..104213268-chr9:104328768..104330503,2	K562	blood:
3	chr9:104332352..104334996-chr9:104342895..104344528,3	MCF-7	breast:
4	chr9:104221051..104221944-chr9:104292075..104293445,6	MCF-7	breast:
5	chr9:104332562..104334673-chr9:104335549..104338409,2	MCF-7	breast:
6	chr9:104211411..104211984-chr9:104329284..104330026,2	MCF-7	breast:
7	chr9:104221444..104221955-chr9:104329285..104330133,2	K562	blood:
8	chr9:104364128..104365110-chr9:107444509..107445032,2	MCF-7	breast:
9	chr9:104292076..104294018-chr9:104296144..104297763,2	K562	blood:
10	chr9:103476641..103477292-chr9:104292118..104293044,2	K562	blood:
11	chr9:104358419..104360916-chr9:104365030..104366580,2	MCF-7	breast:
12	chr9:104220056..104222734-chr9:104292272..104293989,2	K562	blood:
13	chr9:104302143..104304850-chr9:104306401..104308642,2	K562	blood:
14	chr9:104355931..104357895-chr9:104361066..104363280,2	K562	blood:
15	chr9:104220969..104222009-chr9:104292098..104293000,3	K562	blood:
16	chr9:104325829..104329191-chr9:104331276..104334207,4	K562	blood:
17	chr9:104329440..104331713-chr9:104334657..104336622,3	K562	blood:
18	chr9:104303266..104305565-chr9:104316225..104317922,2	K562	blood:
19	chr9:104221464..104223281-chr9:104260800..104263635,2	K562	blood:
20	chr9:104211304..104212259-chr9:104329523..104330518,2	K562	blood:
21	chr9:104303266..104305565-chr9:104316225..104317922,2	K562	blood:
22	chr9:104332562..104334673-chr9:104335549..104338409,2	MCF-7	breast:
23	chr9:104221002..104221801-chr9:104329610..104330484,3	MCF-7	breast:
24	chr9:104358419..104360916-chr9:104365030..104366580,2	MCF-7	breast:
25	chr9:104369041..104371983-chr9:104372682..104374513,2	MCF-7	breast:
26	chr9:104246363..104248786-chr9:104290917..104293044,2	K562	blood:
27	chr9:104219436..104220096-chr9:104292310..104293060,2	MCF-7	breast:
28	chr9:104208004..104209865-chr9:104292464..104295242,2	K562	blood:
29	chr9:104311857..104314554-chr9:104326998..104328848,2	K562	blood:
30	chr9:104302143..104304850-chr9:104306401..104308642,2	K562	blood:
31	chr9:104304678..104307406-chr9:104312351..104313863,2	MCF-7	breast:
32	chr9:104288484..104290134-chr9:104298816..104300608,2	K562	blood:
33	chr9:104210777..104212299-chr9:104292128..104293102,7	MCF-7	breast:
34	chr9:104211181..104212704-chr9:104292065..104293358,10	K562	blood:
35	chr9:104332352..104334996-chr9:104342895..104344528,3	MCF-7	breast:
36	chr9:104295436..104297637-chr9:104304728..104307313,2	K562	blood:
37	chr9:104304678..104307406-chr9:104312351..104313863,2	MCF-7	breast:
38	chr9:104221036..104221738-chr9:104355766..104356658,2	MCF-7	breast:
39	chr9:104226892..104228195-chr9:104292114..104293047,7	MCF-7	breast:
40	chr9:104288484..104290134-chr9:104298816..104300608,2	K562	blood:
41	chr9:104329440..104331713-chr9:104334657..104336622,3	K562	blood:
42	chr9:104325829..104329191-chr9:104331276..104334207,4	K562	blood:
43	chr9:104227401..104228428-chr9:104292031..104293031,5	K562	blood:
44	chr9:104221027..104221969-chr9:104291863..104293035,11	MCF-7	breast:
45	chr9:104295154..104296821-chr9:104298164..104300262,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C9orf125-1	chr9:104295735-104295819	NONHSAT133742
2	lnc-RNF20-3	chr9:104357625-104357790	NONHSAT133747
3	lnc-C9orf125-1	chr9:104293517-104293841	NONHSAT133742
4	lnc-RNF20-3	chr9:104357347-104357370	NONHSAT133747
5	lnc-ALDOB-1	chr9:104263925-104264167	NONHSAT133741
6	lnc-RNF20-3	chr9:104357879-104358148	NONHSAT133747

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	RNF20	hsa-miR-221-3p	chr9:104325139-104325161

Variant related genes	Relation type
ENSG00000233055	TF binding region
RNF20	TF binding region
ENSG00000265068	TF binding region
GRIN3A	TF binding region
TMEM246	TF binding region
PPP3R2	TF binding region
ENSG00000233055	CpG island
RNF20	CpG island
ENSG00000265068	CpG island
GRIN3A	CpG island
TMEM246	CpG island
PPP3R2	CpG island
ENSG00000270982	chromatin interactions
ENSG00000188386	chromatin interactions
ENSG00000265068	chromatin interactions
ENSG00000165152	chromatin interactions
ENSG00000155827	chromatin interactions

Extended variants
information (count: 4618 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:4618 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs572291153	chr9:104263464-104263465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs370262449	chr9:104263465-104263466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs79549425	chr9:104263547-104263548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150876759	chr9:104263558-104263559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs553463262	chr9:104263649-104263650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs374421973	chr9:104263675-104263676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572272415	chr9:104263686-104263687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563025940	chr9:104263754-104263755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1929478	chr9:104263799-104263800	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs551728212	chr9:104263810-104263811	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs559822279	chr9:104263840-104263841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575060015	chr9:104263871-104263872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113271466	chr9:104263928-104263929	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
14	rs116041216	chr9:104263982-104263983	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs547343430	chr9:104263988-104263989	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs567168437	chr9:104263994-104263995	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs186845133	chr9:104264010-104264011	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs190547461	chr9:104264023-104264024	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs369918836	chr9:104264024-104264025	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs575775997	chr9:104264065-104264066	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs538434867	chr9:104264068-104264069	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
22	rs558505929	chr9:104264093-104264094	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
23	rs372514663	chr9:104264173-104264174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs377019874	chr9:104264174-104264175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576269572	chr9:104264175-104264176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554100698	chr9:104264204-104264205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs16920437	chr9:104264211-104264212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs182752231	chr9:104264266-104264267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531876489	chr9:104264328-104264329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368029233	chr9:104264332-104264333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs545564995	chr9:104264342-104264343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs16920438	chr9:104264369-104264370	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs376211270	chr9:104264374-104264375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188853501	chr9:104264433-104264434	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs75073604	chr9:104264458-104264459	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs558998346	chr9:104264464-104264465	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs533365567	chr9:104264482-104264483	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs143017550	chr9:104264484-104264485	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs549403593	chr9:104264497-104264498	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs16920439	chr9:104264540-104264541	Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs146157289	chr9:104264560-104264561	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs193230272	chr9:104264568-104264569	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs565751144	chr9:104264686-104264687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534872439	chr9:104264695-104264696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs184482997	chr9:104264696-104264697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187827186	chr9:104264733-104264734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570281678	chr9:104264760-104264761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs191936984	chr9:104264778-104264779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576580314	chr9:104264795-104264796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs184187056	chr9:104264801-104264802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Melanoma	18172304	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Leukemia	18688285	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute myeloid leukemia	21251322	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Breast cancer	17133270	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Fukuyama congenital muscular dystrophy	21572526	CNVD
Testicular germ cell tumor	18059402	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Mantle cell lymphoma	19029149	CNVD
Intracranial aneurysm	16715129	CNVD
Neuroblastoma	20406844	CNVD
Recurrent pregnancy loss	19789632	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2100 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104263200-104275600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr9:104268000-104268400	Enhancers	HepG2	liver
3	chr9:104269000-104270600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr9:104269400-104271400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr9:104269800-104270800	Enhancers	Adipose Nuclei	Adipose
6	chr9:104269800-104271600	Enhancers	NHDF-Ad	bronchial
7	chr9:104269800-104272200	Enhancers	Fetal Heart	heart
8	chr9:104270000-104271000	Enhancers	NHEK	skin
9	chr9:104270000-104271600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr9:104270000-104271600	Enhancers	NHLF	lung
11	chr9:104270600-104271200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr9:104270600-104274200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:104270800-104271000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
14	chr9:104270800-104276000	Weak transcription	Adipose Nuclei	Adipose
15	chr9:104271000-104276000	Weak transcription	NHEK	skin
16	chr9:104271200-104274200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr9:104271600-104272000	Weak transcription	NHDF-Ad	bronchial
18	chr9:104271600-104274000	Weak transcription	NHLF	lung
19	chr9:104271600-104276000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:104272000-104272600	Enhancers	NHDF-Ad	bronchial
21	chr9:104272200-104274800	Weak transcription	Fetal Heart	heart
22	chr9:104272200-104276400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr9:104272600-104274000	Weak transcription	NHDF-Ad	bronchial
24	chr9:104273400-104277400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr9:104273600-104275600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr9:104273800-104275800	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr9:104274000-104275000	Enhancers	H1 Cell Line	embryonic stem cell
28	chr9:104274000-104275600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr9:104274000-104275800	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr9:104274000-104277200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:104274000-104277200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr9:104274000-104277200	Enhancers	Osteobl	bone
33	chr9:104274000-104277400	Enhancers	NHDF-Ad	bronchial
34	chr9:104274000-104277600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr9:104274000-104277600	Enhancers	NHLF	lung
36	chr9:104274000-104277800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr9:104274200-104274400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
38	chr9:104274200-104274600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr9:104274200-104274800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr9:104274200-104275000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr9:104274200-104277200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr9:104274200-104277200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr9:104274200-104277200	Enhancers	Muscle Satellite Cultured Cells	--
44	chr9:104274400-104274600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr9:104274400-104274600	Enhancers	Aorta	Aorta
46	chr9:104274400-104274600	Enhancers	Pancreas	Pancrea
47	chr9:104274600-104275400	Weak transcription	Aorta	Aorta
48	chr9:104274600-104275800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr9:104274600-104277200	Enhancers	HSMM	muscle
50	chr9:104274600-104277600	Enhancers	H9 Cell Line	embryonic stem cell

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