Variant report

Variant	esv2764161
Chromosome Location	chr9:18247433-18443060
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	ATF2	chr9:18379104-18379511	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr9:18366112-18366540	GM12878	blood:	n/a	n/a
3	ATF3	chr9:18393257-18393736	A549	lung:	n/a	n/a
4	ATF3	chr9:18393238-18393764	HCT-116	colon:	n/a	n/a
5	ATF3	chr9:18393270-18393654	HCT-116	colon:	n/a	n/a
6	BACH1	chr9:18379220-18379436	H1-hESC	embryonic stem cell:	n/a	n/a
7	BCL3	chr9:18393211-18393726	A549	lung:	n/a	n/a
8	BCL3	chr9:18393172-18393686	A549	lung:	n/a	n/a
9	BHLHE40	chr9:18366277-18366484	GM12878	blood:	n/a	n/a
10	BRCA1	chr9:18331838-18332335	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr9:18393063-18394411	Hela-S3	cervix:	n/a	n/a
12	BRCA1	chr9:18437528-18438248	Hela-S3	cervix:	n/a	n/a
13	CBX3	chr9:18393227-18393748	HCT-116	colon:	n/a	n/a
14	CCNT2	chr9:18404527-18404747	K562	blood:	n/a	n/a
15	CEBPB	chr9:18358312-18358647	IMR90	lung:	n/a	n/a
16	CEBPB	chr9:18261187-18261525	IMR90	lung:	n/a	chr9:18261358-18261367 chr9:18261356-18261367 chr9:18261356-18261369 chr9:18261356-18261369 chr9:18261357-18261368
17	CEBPB	chr9:18379082-18379528	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr9:18393265-18393921	IMR90	lung:	n/a	chr9:18393520-18393533
19	CEBPB	chr9:18331665-18332226	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr9:18397643-18397805	HepG2	liver:	n/a	chr9:18397695-18397706
21	CEBPB	chr9:18325717-18325854	H1-hESC	embryonic stem cell:	n/a	chr9:18325794-18325805
22	CEBPB	chr9:18295935-18296021	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr9:18393231-18393839	HCT-116	colon:	n/a	chr9:18393520-18393533
24	CEBPB	chr9:18429159-18429386	HepG2	liver:	n/a	chr9:18429301-18429312
25	CEBPB	chr9:18350992-18351531	HepG2	liver:	n/a	chr9:18351473-18351486
26	CEBPB	chr9:18261193-18261541	Hela-S3	cervix:	n/a	chr9:18261358-18261367 chr9:18261356-18261367 chr9:18261356-18261369 chr9:18261356-18261369 chr9:18261357-18261368
27	CEBPB	chr9:18393319-18393654	ECC-1	luminal epithelium:	n/a	chr9:18393520-18393533
28	CEBPB	chr9:18295836-18296175	IMR90	lung:	n/a	n/a
29	CEBPB	chr9:18379163-18379474	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr9:18393182-18394108	A549	lung:	n/a	chr9:18393520-18393533
31	CEBPB	chr9:18393183-18394289	Hela-S3	cervix:	n/a	chr9:18393520-18393533
32	CEBPB	chr9:18412071-18412407	HepG2	liver:	n/a	chr9:18412243-18412254
33	CEBPB	chr9:18429093-18429510	Hela-S3	cervix:	n/a	chr9:18429301-18429312
34	CEBPB	chr9:18350999-18351315	IMR90	lung:	n/a	n/a
35	CEBPB	chr9:18424146-18424500	HepG2	liver:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
36	CEBPB	chr9:18424148-18424384	HepG2	liver:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
37	CEBPB	chr9:18424197-18424398	HepG2	liver:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
38	CEBPB	chr9:18412122-18412353	Hela-S3	cervix:	n/a	chr9:18412243-18412254
39	CEBPB	chr9:18393291-18393716	A549	lung:	n/a	chr9:18393520-18393533
40	CEBPB	chr9:18379166-18379446	A549	lung:	n/a	n/a
41	CEBPB	chr9:18393266-18393748	A549	lung:	n/a	chr9:18393520-18393533
42	CEBPB	chr9:18325638-18325889	HepG2	liver:	n/a	chr9:18325794-18325805
43	CEBPB	chr9:18325679-18325951	A549	lung:	n/a	chr9:18325794-18325805
44	CEBPB	chr9:18262515-18262577	Hela-S3	cervix:	n/a	chr9:18262548-18262561
45	CEBPB	chr9:18371591-18371841	IMR90	lung:	n/a	chr9:18371712-18371723
46	CEBPB	chr9:18424163-18424437	A549	lung:	n/a	chr9:18424300-18424313 chr9:18424302-18424311 chr9:18424301-18424312 chr9:18424300-18424313 chr9:18424300-18424311
47	CEBPB	chr9:18261210-18261508	A549	lung:	n/a	chr9:18261358-18261367 chr9:18261356-18261367 chr9:18261356-18261369 chr9:18261356-18261369 chr9:18261357-18261368
48	CEBPB	chr9:18325636-18325976	HepG2	liver:	n/a	chr9:18325794-18325805
49	CEBPB	chr9:18387259-18387416	A549	lung:	n/a	n/a
50	CEBPB	chr9:18325607-18325969	IMR90	lung:	n/a	chr9:18325794-18325805

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18437917-18437967	PANC-1	pancreas:	n/a
2	chr9:18437917-18437967	NHBE	bronchial:	n/a
3	chr9:18437917-18437967	PrEC	prostate:	n/a
4	chr9:18437917-18437967	ovcar-3	ovarian:	n/a
5	chr9:18437917-18437967	SKMC	muscle:	n/a
6	chr9:18437917-18437967	Caco-2	colon:	n/a
7	chr9:18437917-18437967	GM12892	blood:	n/a
8	chr9:18437917-18437967	BJ	skin:	n/a
9	chr9:18437917-18437967	AG09309	skin:	n/a
10	chr9:18437917-18437967	GM19239	blood:	n/a
11	chr9:18437917-18437967	MCF10A-Er-Src	breast:	n/a
12	chr9:18437917-18437967	SAEC	small airway:	n/a
13	chr9:18437917-18437967	HRPEpiC	eye:	n/a
14	chr9:18437917-18437967	Hepatocyte	liver:	n/a
15	chr9:18437917-18437967	MCF-7	breast:	n/a
16	chr9:18437917-18437967	SK-N-SH_RA	brain:	n/a
17	chr9:18437917-18437967	SK-N-SH	brain:	n/a
18	chr9:18437917-18437967	AG04450	lung:	fetal
19	chr9:18437917-18437967	HAEpiC	amniotic membrane:	n/a
20	chr9:18437917-18437967	AG04449	skin:	fetal
21	chr9:18437917-18437967	HUVEC	blood vessel:	n/a
22	chr9:18437917-18437967	HL-60	blood:	n/a
23	chr9:18437917-18437967	HCPEpiC	choroid plexus:	n/a
24	chr9:18437917-18437967	Hela-S3	cervix:	n/a
25	chr9:18437917-18437967	NT2-D1	testis:	n/a
26	chr9:18437917-18437967	RPTEC	kidney:	n/a
27	chr9:18437917-18437967	GM06990	blood:	n/a
28	chr9:18437917-18437967	HCT-116	colon:	n/a
29	chr9:18437917-18437967	Jurkat	blood:	n/a
30	chr9:18437917-18437967	AG10803	skin:	n/a
31	chr9:18437917-18437967	HNPCEpiC	eye:	n/a
32	chr9:18437917-18437967	K562	blood:	n/a
33	chr9:18437917-18437967	HCF	heart:	n/a
34	chr9:18437917-18437967	HCM	heart:	n/a
35	chr9:18437917-18437967	HEEpiC	esophagus:	n/a
36	chr9:18437917-18437967	BE2_C	brain:	n/a
37	chr9:18437917-18437967	T-47D	breast:	n/a
38	chr9:18437917-18437967	IMR90	lung:	fetal
39	chr9:18437917-18437967	ProgFib	skin:	n/a
40	chr9:18437917-18437967	U87	brain:	n/a
41	chr9:18437917-18437967	SK-N-MC	brain:	n/a
42	chr9:18437917-18437967	GM12891	blood:	n/a
43	chr9:18437917-18437967	HRCEpiC	kidney:	n/a
44	chr9:18437917-18437967	NH-A	brain:	n/a
45	chr9:18437917-18437967	PFSK-1	brain:	n/a
46	chr9:18437917-18437967	HepG2	liver:	n/a
47	chr9:18437917-18437967	HMEC	breast:	n/a
48	chr9:18437917-18437967	LNCaP	prostate:	n/a
49	chr9:18437917-18437967	HIPEpiC	eye:	n/a
50	chr9:18437917-18437967	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr9:18254805..18255425-chr9:18442379..18443060,2	MCF-7	breast:
2	chr9:18254775..18255482-chr9:18823832..18824683,3	MCF-7	breast:
3	chr9:18436804..18438586-chr9:18439890..18441991,2	MCF-7	breast:
4	chr9:18377972..18379506-chr9:18518837..18521140,2	K562	blood:
5	chr9:18254973..18255762-chr9:19028514..19029097,2	MCF-7	breast:
6	chr9:18254776..18255758-chr9:18790832..18791755,3	MCF-7	breast:
7	chr6:29596747..29597490-chr9:18419651..18420547,2	MCF-7	breast:
8	chr9:18436804..18438586-chr9:18439890..18441991,2	MCF-7	breast:
9	chr13:100230633..100231487-chr9:18324433..18324983,2	MCF-7	breast:
10	chr9:18254805..18255425-chr9:18442379..18443060,2	MCF-7	breast:
11	chr10:103812339..103814566-chr9:18385028..18387430,2	MCF-7	breast:
12	chr9:18255224..18255738-chr9:19028566..19029077,2	K562	blood:
13	chr9:18255104..18255666-chr9:18823787..18824360,2	MCF-7	breast:
14	chr9:18254620..18255832-chr9:18825877..18827696,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM154A-4	chr9:18350595-18350693	NONHSAT130307
2	lnc-FAM154A-2	chr9:18362081-18362218	XLOC_007653
3	lnc-FAM154A-2	chr9:18360595-18360693	XLOC_007653
4	lnc-ADAMTSL1-1	chr9:18283558-18283630	NONHSAT130306
5	lnc-FAM154A-4	chr9:18352081-18352218	NONHSAT130307
6	lnc-ADAMTSL1-1	chr9:18288533-18288954	NONHSAT130306
7	lnc-ADAMTSL1-1	chr9:18290279-18290518	NONHSAT130306

Variant related genes	Relation type
ENSG00000227167	TF binding region
ENSG00000227167	CpG island
ENSG00000178031	chromatin interactions
CPPED1	miRNA target sites
CRAMP1L	miRNA target sites

Extended variants
information (count: 8247 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:8247 , 50 per page) page: 1 2 3 4 5 6 7 ... 165

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568256416	chr9:18247457-18247458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs78677062	chr9:18247464-18247465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555093373	chr9:18247526-18247527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538411846	chr9:18247592-18247593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144823431	chr9:18247638-18247639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147918300	chr9:18247669-18247670	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs10283600	chr9:18247683-18247684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184519651	chr9:18247734-18247735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs189843991	chr9:18247798-18247799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571868165	chr9:18247866-18247867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs141740490	chr9:18247867-18247868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369014136	chr9:18247942-18247943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs374942979	chr9:18247955-18247956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs530363921	chr9:18247982-18247983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs541538176	chr9:18248000-18248001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs368515975	chr9:18248013-18248014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141762096	chr9:18248018-18248019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531529569	chr9:18248028-18248029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs143691786	chr9:18248055-18248056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181397963	chr9:18248062-18248063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564074588	chr9:18248110-18248111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111536233	chr9:18248131-18248132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs11790414	chr9:18248132-18248133	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs559194807	chr9:18248140-18248141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557780460	chr9:18248145-18248146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs11790387	chr9:18248172-18248173	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs577126227	chr9:18248181-18248182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs184476103	chr9:18248206-18248207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs548380162	chr9:18248228-18248229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs570103746	chr9:18248298-18248299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs76532343	chr9:18248328-18248329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs537149171	chr9:18248329-18248330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544269000	chr9:18248340-18248341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533674765	chr9:18248365-18248366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558480844	chr9:18248377-18248378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs576864004	chr9:18248390-18248391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555023561	chr9:18248401-18248402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368307590	chr9:18248429-18248430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188936982	chr9:18248451-18248452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs534980411	chr9:18248457-18248458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs67021093	chr9:18248487-18248488	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs574918718	chr9:18248499-18248500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181674957	chr9:18248563-18248564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563751554	chr9:18248576-18248577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114570316	chr9:18248595-18248596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545923929	chr9:18248600-18248601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs186292984	chr9:18248602-18248603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113373501	chr9:18248630-18248631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528141713	chr9:18248686-18248687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs546897065	chr9:18248705-18248706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Chronic myeloid leukemia	21384125	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	21858162	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Myelofibrosis	22110671	CNVD
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Ovarian cancer	19835627	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1429 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18225800-18260600	Weak transcription	Aorta	Aorta
2	chr9:18250000-18250600	Enhancers	Osteobl	bone
3	chr9:18250200-18250600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr9:18250200-18250600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr9:18250200-18250600	Enhancers	Fetal Heart	heart
6	chr9:18250200-18250600	Enhancers	NH-A	brain
7	chr9:18250200-18250800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr9:18250200-18250800	Enhancers	NHDF-Ad	bronchial
9	chr9:18250400-18250800	Enhancers	NHEK	skin
10	chr9:18250600-18255400	Weak transcription	Fetal Heart	heart
11	chr9:18250600-18255400	Weak transcription	Osteobl	bone
12	chr9:18250600-18255800	Weak transcription	NH-A	brain
13	chr9:18250800-18255400	Weak transcription	NHDF-Ad	bronchial
14	chr9:18250800-18255600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr9:18255000-18255200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr9:18255200-18255400	Bivalent Enhancer	Primary T helper memory cells from peripheral blood 1	blood
17	chr9:18255200-18255600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr9:18255200-18255600	Enhancers	Brain Hippocampus Middle	brain
19	chr9:18255200-18256000	Enhancers	Fetal Stomach	stomach
20	chr9:18255200-18256400	Enhancers	Fetal Kidney	kidney
21	chr9:18255200-18256600	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr9:18255200-18260400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:18255400-18255600	Enhancers	Fetal Brain Male	brain
24	chr9:18255400-18256000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr9:18255400-18256000	Enhancers	HUVEC	blood vessel
26	chr9:18255400-18256200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr9:18255400-18256200	Enhancers	Duodenum Smooth Muscle	Duodenum
28	chr9:18255400-18256600	Enhancers	Colon Smooth Muscle	Colon
29	chr9:18255400-18256600	Enhancers	NHLF	lung
30	chr9:18255400-18256800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr9:18255400-18256800	Enhancers	Fetal Heart	heart
32	chr9:18255400-18256800	Enhancers	Osteobl	bone
33	chr9:18255400-18257000	Enhancers	NHDF-Ad	bronchial
34	chr9:18255600-18256000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr9:18255600-18256000	Enhancers	Fetal Thymus	thymus
36	chr9:18255600-18256800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
37	chr9:18255600-18257000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
38	chr9:18255600-18260000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:18255800-18256200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr9:18255800-18256400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr9:18255800-18256600	Enhancers	NH-A	brain
42	chr9:18256000-18256400	Enhancers	Lung	lung
43	chr9:18256000-18260400	Weak transcription	Muscle Satellite Cultured Cells	--
44	chr9:18256000-18260400	Weak transcription	Fetal Stomach	stomach
45	chr9:18256200-18256600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr9:18256200-18256600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr9:18256200-18256800	Enhancers	Fetal Lung	lung
48	chr9:18256200-18256800	Enhancers	Right Atrium	heart
49	chr9:18256200-18257000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr9:18256200-18261200	Weak transcription	Duodenum Smooth Muscle	Duodenum

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links