Variant report

Variant	esv1009235
Chromosome Location	chr9:27189804-27196618
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	BATF	chr9:27194446-27194714	GM12878	blood:	n/a	chr9:27194607-27194618
2	CBX3	chr9:27194266-27194999	HCT-116	colon:	n/a	n/a
3	CBX3	chr9:27193803-27195211	HCT-116	colon:	n/a	n/a
4	CEBPB	chr9:27194340-27195505	IMR90	lung:	n/a	n/a
5	CEBPB	chr9:27194317-27195157	HCT-116	colon:	n/a	n/a
6	CEBPB	chr9:27194367-27194834	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr9:27194269-27195045	HCT-116	colon:	n/a	n/a
8	CTCF	chr9:27193980-27194130	AG09309	skin:	n/a	n/a
9	E2F4	chr9:27194396-27195229	MCF10A-Er-Src	breast:	n/a	chr9:27194960-27194967 chr9:27194957-27194972 chr9:27194956-27194968 chr9:27194742-27194754 chr9:27194959-27194968 chr9:27194960-27194967 chr9:27194960-27194967
10	E2F4	chr9:27196341-27196655	MCF10A-Er-Src	breast:	n/a	n/a
11	EBF1	chr9:27194448-27194655	GM12878	blood:	n/a	chr9:27194507-27194516
12	EGR1	chr9:27194364-27194990	HCT-116	colon:	n/a	n/a
13	EP300	chr9:27194377-27194725	Hela-S3	cervix:	n/a	n/a
14	EP300	chr9:27194309-27194935	SK-N-SH	brain:	n/a	chr9:27194800-27194810
15	EP300	chr9:27194456-27194706	SK-N-SH_RA	brain:	n/a	n/a
16	FOS	chr9:27196397-27196738	MCF10A-Er-Src	breast:	n/a	n/a
17	FOS	chr9:27196409-27196663	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr9:27194341-27194833	MCF10A-Er-Src	breast:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194583-27194594 chr9:27194610-27194620 chr9:27194614-27194626
19	FOS	chr9:27193931-27195625	MCF10A-Er-Src	breast:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194583-27194594 chr9:27194610-27194620 chr9:27194614-27194626
20	FOS	chr9:27193938-27195492	MCF10A-Er-Src	breast:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194583-27194594 chr9:27194610-27194620 chr9:27194614-27194626
21	FOS	chr9:27195224-27195477	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr9:27196366-27196738	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr9:27193951-27194114	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr9:27196306-27196766	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr9:27193942-27195045	HUVEC	blood vessel:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194583-27194594 chr9:27194610-27194620 chr9:27194614-27194626
26	FOS	chr9:27195194-27195438	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr9:27194406-27194783	MCF10A-Er-Src	breast:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194583-27194594 chr9:27194610-27194620 chr9:27194614-27194626
28	FOSL1	chr9:27193842-27195029	HCT-116	colon:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
29	FOSL1	chr9:27193803-27195107	HCT-116	colon:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
30	FOSL2	chr9:27194403-27194791	SK-N-SH	brain:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
31	FOSL2	chr9:27194003-27194910	SK-N-SH	brain:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
32	GATA3	chr9:27194259-27194865	SK-N-SH	brain:	n/a	n/a
33	JUN	chr9:27193934-27194811	HUVEC	blood vessel:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
34	JUND	chr9:27194228-27194953	HCT-116	colon:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
35	JUND	chr9:27193763-27194959	SK-N-SH	brain:	n/a	chr9:27194083-27194094 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
36	JUND	chr9:27193966-27194933	SK-N-SH	brain:	n/a	chr9:27194083-27194094 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
37	JUND	chr9:27193946-27194855	Hela-S3	cervix:	n/a	chr9:27194083-27194094 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
38	JUND	chr9:27194281-27194914	SK-N-SH	brain:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
39	JUND	chr9:27194292-27195073	HCT-116	colon:	n/a	chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194610-27194620 chr9:27194614-27194626
40	JUND	chr9:27193958-27194158	HepG2	liver:	n/a	chr9:27194083-27194094
41	KAP1	chr9:27194046-27195177	U2OS	brain:	n/a	chr9:27194583-27194592
42	KAP1	chr9:27194517-27194820	HEK293	kidney:	n/a	chr9:27194583-27194592
43	MAFK	chr9:27191647-27191898	HepG2	liver:	n/a	chr9:27191734-27191749
44	MAFK	chr9:27191582-27191847	HepG2	liver:	n/a	chr9:27191734-27191749
45	MAX	chr9:27194354-27195173	HCT-116	colon:	n/a	n/a
46	MAZ	chr9:27194157-27194822	Hela-S3	cervix:	n/a	n/a
47	MXI1	chr9:27196317-27196392	GM12878	blood:	n/a	n/a
48	MYC	chr9:27196370-27196815	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr9:27194474-27194718	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr9:27195276-27195393	MCF10A-Er-Src	breast:	n/a	n/a

Variant related genes	Relation type
RNA5SP280	TF binding region

Extended variants
information (count: 289 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547777161	chr9:27189807-27189808	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566003350	chr9:27189810-27189811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533484847	chr9:27189812-27189813	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs552380888	chr9:27189823-27189824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369987991	chr9:27189833-27189834	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs570696637	chr9:27189837-27189838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538130786	chr9:27189839-27189840	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141603767	chr9:27189847-27189848	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370463702	chr9:27189849-27189850	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375950901	chr9:27189855-27189856	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs140054223	chr9:27189857-27189858	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs568347623	chr9:27189859-27189860	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs139340918	chr9:27189867-27189868	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs10967764	chr9:27189869-27189870	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143221777	chr9:27189871-27189872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545527214	chr9:27189880-27189881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs557920877	chr9:27189896-27189897	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs576276462	chr9:27189932-27189933	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs511586	chr9:27189946-27189947	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs7038775	chr9:27189952-27189953	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs7038890	chr9:27189959-27189960	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs116150807	chr9:27189983-27189984	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377166649	chr9:27190003-27190004	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184612338	chr9:27190046-27190047	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533452174	chr9:27190047-27190048	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188635552	chr9:27190108-27190109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564272467	chr9:27190115-27190116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531490366	chr9:27190120-27190121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549957284	chr9:27190134-27190135	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs150865831	chr9:27190199-27190200	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535764912	chr9:27190211-27190212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs547057490	chr9:27190231-27190232	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs4878361	chr9:27190249-27190250	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs539142274	chr9:27190263-27190264	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181467040	chr9:27190270-27190271	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376776150	chr9:27190291-27190292	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571271185	chr9:27190351-27190352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139528007	chr9:27190395-27190396	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537211203	chr9:27190418-27190419	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs7863225	chr9:27190429-27190430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs375122524	chr9:27190451-27190452	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs369713788	chr9:27190480-27190481	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115012696	chr9:27190492-27190493	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369370428	chr9:27190493-27190494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541747126	chr9:27190505-27190506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371144976	chr9:27190514-27190515	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149684174	chr9:27190545-27190546	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs45607336	chr9:27190553-27190554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs373235916	chr9:27190556-27190557	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200857533	chr9:27190586-27190587	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	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
Oral squamous cell carcinoma	17134496	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
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
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	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
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Epilepsy	22083797	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Lung cancer	20668451	CNVD
Lung adenocarcinoma	21935476	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27151000-27229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:27165400-27198200	Weak transcription	Ovary	ovary
3	chr9:27165400-27219200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr9:27166200-27192200	Weak transcription	Fetal Stomach	stomach
5	chr9:27166200-27205800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr9:27166200-27229000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr9:27178400-27197200	Weak transcription	Fetal Muscle Trunk	muscle
8	chr9:27179600-27191800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr9:27180800-27191800	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr9:27180800-27230600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr9:27182200-27192400	Weak transcription	Fetal Muscle Leg	muscle
12	chr9:27182400-27192200	Weak transcription	Aorta	Aorta
13	chr9:27182400-27192200	Weak transcription	Rectal Smooth Muscle	rectum
14	chr9:27182600-27194000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr9:27184000-27190400	Weak transcription	Left Ventricle	heart
16	chr9:27184000-27192200	Weak transcription	Adipose Nuclei	Adipose
17	chr9:27184000-27197800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr9:27184200-27192600	Weak transcription	Lung	lung
19	chr9:27184200-27193800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr9:27184200-27194000	Weak transcription	Psoas Muscle	Psoas
21	chr9:27184200-27212600	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr9:27184400-27191000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr9:27186000-27192000	Weak transcription	HUVEC	blood vessel
24	chr9:27186400-27190200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr9:27190200-27191200	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr9:27190400-27191000	Strong transcription	Left Ventricle	heart
27	chr9:27191000-27192000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
28	chr9:27191000-27192800	Weak transcription	Left Ventricle	heart
29	chr9:27191200-27192400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:27191800-27192400	Enhancers	Duodenum Smooth Muscle	Duodenum
31	chr9:27191800-27193600	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr9:27192000-27192200	Enhancers	Osteobl	bone
33	chr9:27192000-27192400	Enhancers	Muscle Satellite Cultured Cells	--
34	chr9:27192000-27192800	Enhancers	Colon Smooth Muscle	Colon
35	chr9:27192000-27193200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr9:27192000-27196800	Enhancers	HUVEC	blood vessel
37	chr9:27192200-27192400	Enhancers	NHLF	lung
38	chr9:27192200-27192600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr9:27192200-27193000	Active TSS	Aorta	Aorta
40	chr9:27192200-27193000	Enhancers	Fetal Stomach	stomach
41	chr9:27192200-27193000	Enhancers	Rectal Smooth Muscle	rectum
42	chr9:27192200-27193000	Enhancers	Stomach Smooth Muscle	stomach
43	chr9:27192200-27193000	Enhancers	HSMM	muscle
44	chr9:27192200-27193000	Enhancers	HSMMtube	muscle
45	chr9:27192200-27193400	Enhancers	Adipose Nuclei	Adipose
46	chr9:27192200-27194200	Weak transcription	Osteobl	bone
47	chr9:27192400-27192800	Enhancers	Right Atrium	heart
48	chr9:27192400-27193000	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr9:27192400-27193000	Enhancers	Fetal Muscle Leg	muscle
50	chr9:27192400-27193600	Enhancers	Skeletal Muscle Male	skeletal muscle

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