Variant report

Variant	nsv613726
Chromosome Location	chr9:18676163-18709330
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	chr9:18705112-18705234	K562	blood:	n/a	n/a
2	BACH1	chr9:18708496-18708726	H1-hESC	embryonic stem cell:	n/a	chr9:18708633-18708647
3	CEBPB	chr9:18707184-18707437	IMR90	lung:	n/a	chr9:18707297-18707314
4	CEBPB	chr9:18707301-18707356	K562	blood:	n/a	n/a
5	CEBPB	chr9:18707138-18707487	HepG2	liver:	n/a	chr9:18707297-18707314
6	CEBPB	chr9:18707230-18707376	A549	lung:	n/a	chr9:18707297-18707314
7	CEBPB	chr9:18699795-18700171	Hela-S3	cervix:	n/a	n/a
8	CHD2	chr9:18707401-18707405	HepG2	liver:	n/a	n/a
9	CTCF	chr9:18703160-18703310	AG04450	lung:	n/a	chr9:18703274-18703292
10	CTCF	chr9:18695083-18695172	Kidney_OC	kidney:	n/a	n/a
11	CTCF	chr9:18699567-18699611	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr9:18703260-18703410	AG04450	lung:	n/a	chr9:18703274-18703292
13	CTCF	chr9:18703180-18703330	HCPEpiC	choroid plexus:	n/a	chr9:18703274-18703292
14	CTCF	chr9:18703340-18703490	NHDF-neo	bronchial:	n/a	n/a
15	CTCF	chr9:18703240-18703390	AG04449	skin:	n/a	chr9:18703274-18703292
16	CTCF	chr9:18703360-18703510	NHDF-neo	bronchial:	n/a	n/a
17	CTCF	chr9:18703180-18703330	HPAF	blood vessel:	n/a	chr9:18703274-18703292
18	CTCF	chr9:18703180-18703330	SK-N-SH_RA	brain:	n/a	chr9:18703274-18703292
19	CTCF	chr9:18703240-18703390	HPF	lung:	n/a	chr9:18703274-18703292
20	CTCF	chr9:18703160-18703310	AG09309	skin:	n/a	chr9:18703274-18703292
21	CTCF	chr9:18703160-18703310	AoAF	blood vessel:	n/a	chr9:18703274-18703292
22	CTCF	chr9:18701979-18702050	GM10248	blood:	n/a	n/a
23	CTCF	chr9:18703160-18703310	HCPEpiC	choroid plexus:	n/a	chr9:18703274-18703292
24	CTCF	chr9:18703180-18703330	AG09319	gingival:	n/a	chr9:18703274-18703292
25	CTCF	chr9:18703240-18703390	HCM	heart:	n/a	chr9:18703274-18703292
26	CTCF	chr9:18703220-18703370	HCM	heart:	n/a	chr9:18703274-18703292
27	CTCF	chr9:18703180-18703330	HBMEC	blood vessel:	n/a	chr9:18703274-18703292
28	E2F4	chr9:18688874-18689131	MCF10A-Er-Src	breast:	n/a	n/a
29	EP300	chr9:18699888-18700124	Hela-S3	cervix:	n/a	n/a
30	EP300	chr9:18703325-18703666	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr9:18692235-18692704	SK-N-SH_RA	brain:	n/a	chr9:18692686-18692700
32	EP300	chr9:18692252-18692627	SK-N-SH_RA	brain:	n/a	n/a
33	FOS	chr9:18678974-18679202	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr9:18689266-18689554	HUVEC	blood vessel:	n/a	n/a
35	FOS	chr9:18699853-18700132	MCF10A-Er-Src	breast:	n/a	n/a
36	FOXM1	chr9:18692186-18692625	GM12878	blood:	n/a	n/a
37	GATA2	chr9:18703025-18704285	SH-SY5Y	brain:	n/a	chr9:18703931-18703938 chr9:18703389-18703396 chr9:18703565-18703574 chr9:18703931-18703938 chr9:18703931-18703938 chr9:18703560-18703581
38	GATA2	chr9:18692864-18693367	SH-SY5Y	brain:	n/a	n/a
39	GATA2	chr9:18706959-18707416	SH-SY5Y	brain:	n/a	chr9:18707142-18707151
40	GATA3	chr9:18691811-18692166	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr9:18703738-18704289	SK-N-SH	brain:	n/a	chr9:18703931-18703938 chr9:18703931-18703938 chr9:18703931-18703938
42	GATA3	chr9:18691121-18691456	SH-SY5Y	brain:	n/a	chr9:18691269-18691279 chr9:18691269-18691278 chr9:18691271-18691278 chr9:18691271-18691278 chr9:18691266-18691282 chr9:18691271-18691278 chr9:18691264-18691285 chr9:18691235-18691242 chr9:18691271-18691281
43	GATA3	chr9:18693046-18693244	T-47D	breast:	n/a	n/a
44	GATA3	chr9:18703293-18704323	SH-SY5Y	brain:	n/a	chr9:18703931-18703938 chr9:18703389-18703396 chr9:18703565-18703574 chr9:18703931-18703938 chr9:18703931-18703938 chr9:18703560-18703581
45	GATA3	chr9:18687372-18687510	SH-SY5Y	brain:	n/a	n/a
46	GATA3	chr9:18692846-18693461	SH-SY5Y	brain:	n/a	chr9:18693446-18693456
47	GATA3	chr9:18700996-18701196	SH-SY5Y	brain:	n/a	n/a
48	IRF1	chr9:18708819-18708851	K562	blood:	n/a	n/a
49	JUND	chr9:18708498-18708584	H1-hESC	embryonic stem cell:	n/a	n/a
50	KAP1	chr9:18675337-18676296	U2OS	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:18706865-18706915	MCF10A-Er-Src	breast:	n/a
2	chr9:18706865-18706915	NHBE	bronchial:	n/a
3	chr9:18706865-18706915	HAEpiC	amniotic membrane:	n/a
4	chr9:18706865-18706915	HepG2	liver:	n/a
5	chr9:18706865-18706915	U87	brain:	n/a
6	chr9:18706865-18706915	HNPCEpiC	eye:	n/a
7	chr9:18706865-18706915	NH-A	brain:	n/a
8	chr9:18706865-18706915	ProgFib	skin:	n/a
9	chr9:18706865-18706915	SK-N-SH_RA	brain:	n/a
10	chr9:18706865-18706915	BE2_C	brain:	n/a
11	chr9:18706865-18706915	HL-60	blood:	n/a
12	chr9:18706865-18706915	PrEC	prostate:	n/a
13	chr9:18706865-18706915	ovcar-3	ovarian:	n/a
14	chr9:18706865-18706915	PFSK-1	brain:	n/a
15	chr9:18706865-18706915	BJ	skin:	n/a
16	chr9:18706865-18706915	HRE	kidney:	n/a
17	chr9:18706865-18706915	RPTEC	kidney:	n/a
18	chr9:18706865-18706915	AoSMC	blood vessel:	n/a
19	chr9:18706865-18706915	SK-N-SH	brain:	n/a
20	chr9:18706865-18706915	AG04449	skin:	fetal
21	chr9:18706865-18706915	PANC-1	pancreas:	n/a
22	chr9:18706865-18706915	HIPEpiC	eye:	n/a
23	chr9:18706865-18706915	A549	lung:	n/a
24	chr9:18706865-18706915	HCPEpiC	choroid plexus:	n/a
25	chr9:18706865-18706915	GM19239	blood:	n/a
26	chr9:18706865-18706915	HRCEpiC	kidney:	n/a
27	chr9:18706865-18706915	AG09309	skin:	n/a
28	chr9:18706865-18706915	HEK293	kidney:	embryo
29	chr9:18706865-18706915	HUVEC	blood vessel:	n/a
30	chr9:18706865-18706915	GM12891	blood:	n/a
31	chr9:18706865-18706915	SAEC	small airway:	n/a
32	chr9:18706865-18706915	SKMC	muscle:	n/a
33	chr9:18706865-18706915	ECC-1	luminal epithelium:	n/a
34	chr9:18706865-18706915	SK-N-MC	brain:	n/a
35	chr9:18706865-18706915	AG09319	gingival:	n/a
36	chr9:18706865-18706915	HMEC	breast:	n/a
37	chr9:18706865-18706915	HPAEpiC	pulmonary alveolar:	n/a
38	chr9:18706865-18706915	Hela-S3	cervix:	n/a
39	chr9:18706865-18706915	AG10803	skin:	n/a
40	chr9:18706865-18706915	LNCaP	prostate:	n/a
41	chr9:18706865-18706915	HRPEpiC	eye:	n/a
42	chr9:18706865-18706915	MCF-7	breast:	n/a
43	chr9:18706865-18706915	K562	blood:	n/a
44	chr9:18706865-18706915	AG04450	lung:	fetal
45	chr9:18706865-18706915	Caco-2	colon:	n/a
46	chr9:18706865-18706915	HCM	heart:	n/a
47	chr9:18706865-18706915	HEEpiC	esophagus:	n/a
48	chr9:18706865-18706915	H1-hESC	embryonic stem cell:	embryo
49	chr9:18706865-18706915	GM12892	blood:	n/a
50	chr9:18706865-18706915	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr21:39358274..39359037-chr9:18704805..18705621,2	MCF-7	breast:
2	chr8:61562599..61565494-chr9:18702295..18704681,2	MCF-7	breast:
3	chr9:18705469..18707872-chr9:18709248..18712015,2	MCF-7	breast:

No.	miRNA target gene	miRNA name	Chromosome Location
1	ADAMTSL1	hsa-miR-25-3p	chr9:18681248-18681269
2	ADAMTSL1	hsa-miR-132-3p	chr9:18684803-18684824
3	ADAMTSL1	hsa-miR-25-3p	chr9:18681336-18681357

Variant related genes	Relation type
ADAMTSL1	TF binding region
ADAMTSL1	CpG island
ENSG00000178031	chromatin interactions

Extended variants
information (count: 1383 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:1383 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs776764	chr9:18676163-18676164	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs776763	chr9:18676211-18676212	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs550186282	chr9:18676233-18676234	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs535986174	chr9:18676376-18676377	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555888838	chr9:18676391-18676392	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs574155065	chr9:18676401-18676402	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568541180	chr9:18676413-18676414	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141016997	chr9:18676414-18676415	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs578259062	chr9:18676460-18676461	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs545400496	chr9:18676468-18676469	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs34312083	chr9:18676481-18676482	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs113458206	chr9:18676489-18676490	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2487477	chr9:18676496-18676497	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs34220297	chr9:18676544-18676545	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs148245172	chr9:18676580-18676581	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs16936960	chr9:18676659-18676660	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs187810564	chr9:18676733-18676734	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs566442029	chr9:18676757-18676758	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs776762	chr9:18676798-18676799	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs546909515	chr9:18676837-18676838	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571516742	chr9:18676862-18676863	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs571192044	chr9:18676902-18676903	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs7045779	chr9:18676945-18676946	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs140235038	chr9:18676965-18676966	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs80352342	chr9:18676991-18676992	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs192607434	chr9:18676992-18676993	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs376446527	chr9:18677006-18677007	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554365658	chr9:18677047-18677048	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574006111	chr9:18677114-18677115	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569773744	chr9:18677118-18677119	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547345801	chr9:18677147-18677148	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558294982	chr9:18677226-18677227	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs117490287	chr9:18677292-18677293	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372554913	chr9:18677310-18677311	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs77706790	chr9:18677337-18677338	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs7018593	chr9:18677372-18677373	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs554092593	chr9:18677445-18677446	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556479369	chr9:18677464-18677465	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116859583	chr9:18677469-18677470	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs369673601	chr9:18677473-18677474	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567054809	chr9:18677549-18677550	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77455526	chr9:18677591-18677592	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7019258	chr9:18677654-18677655	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs184450687	chr9:18677655-18677656	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116145371	chr9:18677683-18677684	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs78950815	chr9:18677710-18677711	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137935669	chr9:18677718-18677719	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs560636845	chr9:18677723-18677724	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs529650278	chr9:18677759-18677760	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs548204206	chr9:18677764-18677765	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Glycine encephalopathy	21572526	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Cancer	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Myelofibrosis	22110671	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:360 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18648200-18683200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr9:18658600-18680000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr9:18666800-18680000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr9:18667600-18690800	Weak transcription	Aorta	Aorta
5	chr9:18672600-18679800	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr9:18673000-18676200	Enhancers	Fetal Heart	heart
7	chr9:18673600-18676400	Weak transcription	NH-A	brain
8	chr9:18674800-18676200	Enhancers	Fetal Lung	lung
9	chr9:18675000-18677200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr9:18675200-18676200	Enhancers	HSMMtube	muscle
11	chr9:18675200-18677200	Enhancers	Adipose Nuclei	Adipose
12	chr9:18675200-18679800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr9:18675400-18676200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr9:18675400-18678800	Weak transcription	Fetal Stomach	stomach
15	chr9:18675600-18678800	Weak transcription	Colon Smooth Muscle	Colon
16	chr9:18675600-18679000	Strong transcription	NHDF-Ad	bronchial
17	chr9:18675600-18688800	Weak transcription	HUVEC	blood vessel
18	chr9:18675600-18695000	Weak transcription	NHLF	lung
19	chr9:18675800-18710000	Strong transcription	HSMM	muscle
20	chr9:18676000-18676200	Enhancers	Fetal Kidney	kidney
21	chr9:18676000-18676600	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr9:18676000-18677400	Enhancers	Osteobl	bone
23	chr9:18676000-18678800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr9:18676200-18676600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr9:18676200-18676600	Weak transcription	HSMMtube	muscle
26	chr9:18676200-18678800	Weak transcription	Fetal Kidney	kidney
27	chr9:18676200-18678800	Weak transcription	Fetal Lung	lung
28	chr9:18676200-18690800	Weak transcription	Fetal Heart	heart
29	chr9:18676400-18677000	Strong transcription	NH-A	brain
30	chr9:18676600-18676800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr9:18676600-18676800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr9:18676600-18676800	Enhancers	HSMMtube	muscle
33	chr9:18676800-18677000	Weak transcription	Muscle Satellite Cultured Cells	--
34	chr9:18676800-18684600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
35	chr9:18676800-18692000	Weak transcription	HSMMtube	muscle
36	chr9:18677000-18677200	Genic enhancers	Muscle Satellite Cultured Cells	--
37	chr9:18677000-18679400	Weak transcription	NH-A	brain
38	chr9:18677200-18678600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr9:18677200-18678800	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr9:18677200-18678800	Weak transcription	Adipose Nuclei	Adipose
41	chr9:18677400-18678000	Weak transcription	Osteobl	bone
42	chr9:18678000-18679600	Enhancers	Osteobl	bone
43	chr9:18678600-18679800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr9:18678800-18679000	Enhancers	Fetal Kidney	kidney
45	chr9:18678800-18679000	Enhancers	Ovary	ovary
46	chr9:18678800-18679200	Enhancers	Fetal Stomach	stomach
47	chr9:18678800-18679400	Enhancers	Muscle Satellite Cultured Cells	--
48	chr9:18678800-18679800	Enhancers	Adipose Nuclei	Adipose
49	chr9:18678800-18679800	Enhancers	Colon Smooth Muscle	Colon
50	chr9:18678800-18679800	Enhancers	Fetal Lung	lung

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