Variant report

Variant	nsv4131
Chromosome Location	chr3:177366549-177399301
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:256)
CpG islands
(count:183)
Chromatin interactive
region (count:7)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:177390113-177390416	K562	blood:	n/a	n/a
2	ARID3A	chr3:177397308-177397855	K562	blood:	n/a	n/a
3	ATF1	chr3:177391194-177391497	K562	blood:	n/a	n/a
4	ATF1	chr3:177397467-177397852	K562	blood:	n/a	n/a
5	BACH1	chr3:177391146-177391645	K562	blood:	n/a	n/a
6	BHLHE40	chr3:177390263-177390600	K562	blood:	n/a	n/a
7	BHLHE40	chr3:177391226-177391567	K562	blood:	n/a	n/a
8	CBX3	chr3:177397458-177397874	K562	blood:	n/a	n/a
9	CBX3	chr3:177382598-177382939	K562	blood:	n/a	n/a
10	CBX3	chr3:177391170-177391815	K562	blood:	n/a	n/a
11	CCNT2	chr3:177397475-177397861	K562	blood:	n/a	n/a
12	CCNT2	chr3:177390121-177390597	K562	blood:	n/a	n/a
13	CEBPB	chr3:177374127-177374480	HepG2	liver:	n/a	chr3:177374156-177374164
14	CEBPB	chr3:177397876-177398314	IMR90	lung:	n/a	chr3:177398008-177398021
15	CEBPB	chr3:177374151-177374450	A549	lung:	n/a	chr3:177374156-177374164
16	CEBPB	chr3:177374103-177374505	ECC-1	luminal epithelium:	n/a	chr3:177374156-177374164
17	CEBPB	chr3:177391160-177391441	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:177389350-177389402	K562	blood:	n/a	n/a
19	CEBPB	chr3:177397873-177398306	Hela-S3	cervix:	n/a	chr3:177398008-177398021
20	CEBPB	chr3:177374197-177374357	HepG2	liver:	n/a	n/a
21	CEBPB	chr3:177398012-177398353	K562	blood:	n/a	n/a
22	CEBPB	chr3:177374198-177374444	K562	blood:	n/a	n/a
23	CEBPB	chr3:177374188-177374423	IMR90	lung:	n/a	n/a
24	CEBPB	chr3:177382897-177383262	MCF-7	breast:	n/a	n/a
25	CEBPB	chr3:177394716-177394936	HepG2	liver:	n/a	chr3:177394909-177394917 chr3:177394797-177394808
26	CEBPD	chr3:177389968-177390506	K562	blood:	n/a	n/a
27	CTCF	chr3:177382276-177382394	GM12878	blood:	n/a	n/a
28	CTCF	chr3:177382160-177382310	RPTEC	kidney:	n/a	n/a
29	CTCF	chr3:177382220-177382370	GM12873	blood:	n/a	n/a
30	CTCF	chr3:177382160-177382310	GM12870	blood:	n/a	n/a
31	CTCF	chr3:177382268-177382406	MCF-7	breast:	n/a	n/a
32	CTCF	chr3:177382276-177382403	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:177382315-177382419	GM10266	blood:	n/a	n/a
34	CTCF	chr3:177382280-177382404	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:177382290-177382395	K562	blood:	n/a	n/a
36	CTCF	chr3:177382200-177382350	GM12872	blood:	n/a	n/a
37	CTCF	chr3:177382260-177382408	MCF-7	breast:	n/a	n/a
38	CTCF	chr3:177398000-177398150	AoAF	blood vessel:	n/a	chr3:177398016-177398029
39	CTCF	chr3:177394320-177394470	RPTEC	kidney:	n/a	n/a
40	CTCF	chr3:177382314-177382380	HepG2	liver:	n/a	n/a
41	CTCF	chr3:177382268-177382397	GM12892	blood:	n/a	n/a
42	CTCF	chr3:177382420-177382570	GM12873	blood:	n/a	n/a
43	CTCF	chr3:177382160-177382310	GM12865	blood:	n/a	n/a
44	CTCF	chr3:177382255-177382405	MCF-7	breast:	n/a	n/a
45	CTCF	chr3:177397700-177397850	BE2_C	brain:	n/a	n/a
46	CTCF	chr3:177382296-177382387	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr3:177397800-177397950	HPAF	blood vessel:	n/a	chr3:177397922-177397940
48	CTCF	chr3:177382264-177382464	GM12891	blood:	n/a	n/a
49	CTCF	chr3:177382271-177382406	GM19240	blood:	n/a	n/a
50	CTCF	chr3:177382308-177382377	A549	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:177370839-177370889	HCT-116	colon:	n/a
2	chr3:177397780-177397830	K562	blood:	n/a
3	chr3:177370839-177370889	GM12892	blood:	n/a
4	chr3:177391387-177391437	GM12892	blood:	n/a
5	chr3:177397780-177397830	HIPEpiC	eye:	n/a
6	chr3:177370839-177370889	RPTEC	kidney:	n/a
7	chr3:177397780-177397830	HPAEpiC	pulmonary alveolar:	n/a
8	chr3:177391387-177391437	ProgFib	skin:	n/a
9	chr3:177370839-177370889	H1-hESC	embryonic stem cell:	embryo
10	chr3:177370839-177370889	NT2-D1	testis:	n/a
11	chr3:177391387-177391437	HUVEC	blood vessel:	n/a
12	chr3:177397780-177397830	HUVEC	blood vessel:	n/a
13	chr3:177370839-177370889	HRPEpiC	eye:	n/a
14	chr3:177391387-177391437	H1-hESC	embryonic stem cell:	embryo
15	chr3:177391387-177391437	BJ	skin:	n/a
16	chr3:177397780-177397830	HRE	kidney:	n/a
17	chr3:177370839-177370889	HCM	heart:	n/a
18	chr3:177370839-177370889	GM12891	blood:	n/a
19	chr3:177370839-177370889	U87	brain:	n/a
20	chr3:177391387-177391437	Hela-S3	cervix:	n/a
21	chr3:177397780-177397830	NHDF-neo	bronchial:	n/a
22	chr3:177391387-177391437	GM06990	blood:	n/a
23	chr3:177370839-177370889	SK-N-SH	brain:	n/a
24	chr3:177397780-177397830	PFSK-1	brain:	n/a
25	chr3:177391387-177391437	HEK293	kidney:	embryo
26	chr3:177391387-177391437	PANC-1	pancreas:	n/a
27	chr3:177397780-177397830	PrEC	prostate:	n/a
28	chr3:177370839-177370889	BJ	skin:	n/a
29	chr3:177397780-177397830	SK-N-SH_RA	brain:	n/a
30	chr3:177397780-177397830	Hela-S3	cervix:	n/a
31	chr3:177397780-177397830	MCF-7	breast:	n/a
32	chr3:177397780-177397830	Hepatocyte	liver:	n/a
33	chr3:177370839-177370889	SKMC	muscle:	n/a
34	chr3:177391387-177391437	NB4	blood:	n/a
35	chr3:177397780-177397830	AG09309	skin:	n/a
36	chr3:177370839-177370889	HEK293	kidney:	embryo
37	chr3:177397780-177397830	SK-N-SH	brain:	n/a
38	chr3:177397780-177397830	GM12878	blood:	n/a
39	chr3:177397780-177397830	SKMC	muscle:	n/a
40	chr3:177370839-177370889	NHDF-neo	bronchial:	n/a
41	chr3:177397780-177397830	HCPEpiC	choroid plexus:	n/a
42	chr3:177397780-177397830	GM12892	blood:	n/a
43	chr3:177397780-177397830	AG04450	lung:	fetal
44	chr3:177391387-177391437	AoSMC	blood vessel:	n/a
45	chr3:177391387-177391437	SKMC	muscle:	n/a
46	chr3:177370839-177370889	HUVEC	blood vessel:	n/a
47	chr3:177391387-177391437	HNPCEpiC	eye:	n/a
48	chr3:177370839-177370889	NB4	blood:	n/a
49	chr3:177397780-177397830	ECC-1	luminal epithelium:	n/a
50	chr3:177370839-177370889	Hepatocyte	liver:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:177381786..177384467-chr3:177540432..177542269,2	MCF-7	breast:
2	chr3:177396417..177398253-chr3:177403984..177405833,2	MCF-7	breast:
3	chr3:177359797..177361546-chr3:177370078..177371976,2	K562	blood:
4	chr3:176875816..176877609-chr3:177391854..177394019,2	MCF-7	breast:
5	chr3:177395868..177398215-chr3:177400550..177402752,2	MCF-7	breast:
6	chr3:177381922..177383460-chr3:177528159..177530120,2	MCF-7	breast:
7	chr3:177398506..177400476-chr3:177405856..177408346,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNMB2-13	chr3:177369326-177369418	NONHSAT093352
2	lnc-KCNMB2-13	chr3:177372254-177372681	NONHSAT093352
3	lnc-KCNMB2-5	chr3:177394498-177394794	ENSG00000228221

No data

Variant related genes	Relation type
LINC00578	TF binding region
ENSG00000228561	TF binding region
LINC00578	CpG island
ENSG00000228561	CpG island
ENSG00000228561	chromatin interactions

Extended variants
information (count: 1172 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1172 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545501844	chr3:177366558-177366559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs565111688	chr3:177366561-177366562	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184945991	chr3:177366566-177366567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs531014740	chr3:177366576-177366577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs17571915	chr3:177366578-177366579	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs376834036	chr3:177366634-177366635	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs529617442	chr3:177366638-177366639	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs546309790	chr3:177366730-177366731	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs376147432	chr3:177366773-177366774	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs111794145	chr3:177366781-177366782	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566479025	chr3:177366789-177366790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs147993603	chr3:177366791-177366792	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189449121	chr3:177366794-177366795	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs150226987	chr3:177366838-177366839	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192435075	chr3:177366840-177366841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377618016	chr3:177366855-177366856	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs76127859	chr3:177366856-177366857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184854508	chr3:177366907-177366908	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532976339	chr3:177367110-177367111	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs138708083	chr3:177367132-177367133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148933184	chr3:177367154-177367155	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs536633982	chr3:177367199-177367200	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189331361	chr3:177367240-177367241	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145531222	chr3:177367282-177367283	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs16828417	chr3:177367351-177367352	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs558665416	chr3:177367379-177367380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181986953	chr3:177367389-177367390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544428574	chr3:177367405-177367406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs561227699	chr3:177367407-177367408	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs79016550	chr3:177367424-177367425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs540943280	chr3:177367440-177367441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185906481	chr3:177367464-177367465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs532142351	chr3:177367552-177367553	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190019776	chr3:177367572-177367573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs142517995	chr3:177367584-177367585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62282544	chr3:177367616-177367617	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569787383	chr3:177367634-177367635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs181264252	chr3:177367689-177367690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568280091	chr3:177367738-177367739	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533820646	chr3:177367850-177367851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs186521703	chr3:177367860-177367861	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554039651	chr3:177367868-177367869	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566714313	chr3:177367874-177367875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs539068983	chr3:177367937-177367938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs1499808	chr3:177367964-177367965	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs190936782	chr3:177367985-177367986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549544038	chr3:177367987-177367988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544313329	chr3:177368006-177368007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554715333	chr3:177368026-177368027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs182303803	chr3:177368059-177368060	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Basal cell lymphoma	21115979	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16608533	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-small cell lung cancer	19010865	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	21785460	CNVD
Breast cancer	17133270	CNVD
epilepsy	18472482	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Myxofibrosarcoma	16751306	CNVD
Parkinson disease	21907011	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Anaplastic thyroid cancer	17989125	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Ovarian cancer	18208621	CNVD
Thyroid cancer	17317825	CNVD
Thyroid cancer	17989125	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	21806811	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	16751803	CNVD
abnormal development	18461090	CNVD
lymphocytic leukemia	21291569	CNVD
Autism	19653912	CNVD
Cancer	20164920	CNVD
Endometrial cancer	19261849	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Esophageal squamous carcinoma	17470683	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:371 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:177360600-177369600	Weak transcription	Fetal Brain Female	brain
2	chr3:177360800-177367000	Enhancers	Primary T killer memory cells from peripheral blood	blood
3	chr3:177360800-177367200	Enhancers	Primary T helper naive cells from peripheral blood	blood
4	chr3:177361000-177369800	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr3:177361400-177367200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
6	chr3:177363000-177369600	Weak transcription	Fetal Kidney	kidney
7	chr3:177363400-177366800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
8	chr3:177363600-177366800	Enhancers	Primary T helper cells fromperipheralblood	blood
9	chr3:177363800-177366800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr3:177363800-177367000	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr3:177364400-177366600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
12	chr3:177364400-177367000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
13	chr3:177364600-177367200	Enhancers	Primary T cells fromperipheralblood	blood
14	chr3:177364600-177367200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
15	chr3:177364800-177369800	Weak transcription	Colon Smooth Muscle	Colon
16	chr3:177364800-177370800	Weak transcription	Psoas Muscle	Psoas
17	chr3:177365200-177366600	Enhancers	Thymus	Thymus
18	chr3:177365800-177370800	Weak transcription	Aorta	Aorta
19	chr3:177366000-177367200	Enhancers	Dnd41	blood
20	chr3:177366000-177368000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
21	chr3:177366000-177369800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr3:177366800-177370000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
23	chr3:177367000-177370000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
24	chr3:177367200-177369400	Weak transcription	Primary T cells fromperipheralblood	blood
25	chr3:177367200-177370000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
26	chr3:177367200-177371000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
27	chr3:177368000-177368200	Weak transcription	Fetal Heart	heart
28	chr3:177368000-177368200	Enhancers	Rectal Smooth Muscle	rectum
29	chr3:177368200-177368400	Enhancers	Fetal Heart	heart
30	chr3:177368200-177368400	Enhancers	HSMMtube	muscle
31	chr3:177368400-177369600	Weak transcription	Fetal Heart	heart
32	chr3:177368400-177369800	Weak transcription	Rectal Smooth Muscle	rectum
33	chr3:177369400-177369600	Enhancers	Left Ventricle	heart
34	chr3:177369400-177370200	Enhancers	Primary T cells fromperipheralblood	blood
35	chr3:177369400-177370600	Weak transcription	HSMMtube	muscle
36	chr3:177369400-177371000	Enhancers	Fetal Brain Male	brain
37	chr3:177369600-177370800	Weak transcription	Left Ventricle	heart
38	chr3:177369600-177371000	Enhancers	Fetal Brain Female	brain
39	chr3:177369600-177371200	Enhancers	Fetal Heart	heart
40	chr3:177369600-177371400	Enhancers	Fetal Kidney	kidney
41	chr3:177369600-177371400	Enhancers	Fetal Lung	lung
42	chr3:177369800-177370200	Enhancers	Brain Angular Gyrus	brain
43	chr3:177369800-177370200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr3:177369800-177370400	Enhancers	Brain Anterior Caudate	brain
45	chr3:177369800-177371000	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr3:177369800-177371000	Enhancers	Colon Smooth Muscle	Colon
47	chr3:177369800-177371400	Enhancers	Rectal Smooth Muscle	rectum
48	chr3:177370000-177370200	Enhancers	Brain Hippocampus Middle	brain
49	chr3:177370000-177370200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
50	chr3:177370000-177370600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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