Variant report

Variant	nsv877346
Chromosome Location	chr3:112893640-112938683
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:357)
CpG islands
(count:1589)
Chromatin interactive
region (count:16)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr3:112931290-112931581	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr3:112930587-112930930	H1-hESC	embryonic stem cell:	n/a	chr3:112930861-112930875
3	BACH1	chr3:112929513-112929539	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr3:112929519-112929712	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr3:112919826-112920174	H1-hESC	embryonic stem cell:	n/a	chr3:112919984-112919995
6	CEBPB	chr3:112894086-112894166	HepG2	liver:	n/a	chr3:112894106-112894117 chr3:112894105-112894118 chr3:112894105-112894116 chr3:112894105-112894116
7	CEBPB	chr3:112919811-112920177	IMR90	lung:	n/a	chr3:112919984-112919995
8	CEBPB	chr3:112919820-112920163	Hela-S3	cervix:	n/a	chr3:112919984-112919995
9	CEBPB	chr3:112919835-112920164	HepG2	liver:	n/a	chr3:112919984-112919995
10	CEBPB	chr3:112919801-112920179	A549	lung:	n/a	chr3:112919984-112919995
11	CEBPB	chr3:112919799-112920234	MCF-7	breast:	n/a	chr3:112919984-112919995
12	CEBPB	chr3:112919697-112920293	A549	lung:	n/a	chr3:112919984-112919995
13	CEBPB	chr3:112924454-112924701	MCF-7	breast:	n/a	n/a
14	CEBPB	chr3:112919905-112920180	A549	lung:	n/a	chr3:112919984-112919995
15	CEBPB	chr3:112929490-112929663	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr3:112893675-112894297	IMR90	lung:	n/a	chr3:112894106-112894117 chr3:112894105-112894118 chr3:112894105-112894116 chr3:112894105-112894116 chr3:112893734-112893745 chr3:112893736-112893745
17	CHD1	chr3:112929934-112930238	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD1	chr3:112930818-112930958	H1-hESC	embryonic stem cell:	n/a	chr3:112930937-112930947
19	CHD1	chr3:112931173-112931260	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD1	chr3:112929519-112929521	H1-hESC	embryonic stem cell:	n/a	n/a
21	CHD2	chr3:112929356-112929657	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTBP2	chr3:112929701-112931583	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr3:112932820-112932970	AG10803	skin:	n/a	n/a
24	CTCF	chr3:112930840-112930990	NHEK	skin:	n/a	n/a
25	CTCF	chr3:112932852-112932864	Fibrobl	skin:	n/a	n/a
26	CTCF	chr3:112930803-112931052	IMR90	lung:	n/a	n/a
27	CTCF	chr3:112931740-112931890	BJ	skin:	n/a	n/a
28	CTCF	chr3:112934414-112934452	Lung_OC	lung:	n/a	n/a
29	CTCF	chr3:112930820-112930970	HepG2	liver:	n/a	n/a
30	CTCF	chr3:112930602-112930609	MCF-7	breast:	n/a	n/a
31	CTCF	chr3:112932816-112932961	NHEK	skin:	n/a	n/a
32	CTCF	chr3:112930820-112930970	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr3:112930840-112930990	HCFaa	heart:	n/a	n/a
34	CTCF	chr3:112933220-112933370	GM12871	blood:	n/a	n/a
35	CTCF	chr3:112931540-112931690	NHEK	skin:	n/a	n/a
36	CTCF	chr3:112930820-112930970	AG04449	skin:	n/a	n/a
37	CTCF	chr3:112930840-112930990	HPAF	blood vessel:	n/a	n/a
38	CTCF	chr3:112930931-112931015	Fibrobl	skin:	n/a	n/a
39	CTCF	chr3:112930938-112930991	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:112933160-112933310	NHEK	skin:	n/a	n/a
41	CTCF	chr3:112930961-112930984	ProgFib	skin:	n/a	n/a
42	CTCF	chr3:112932780-112932930	AG10803	skin:	n/a	n/a
43	CTCF	chr3:112933200-112933350	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr3:112930720-112930870	GM12873	blood:	n/a	n/a
45	CTCF	chr3:112930956-112930989	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr3:112932840-112932990	HMF	breast:	n/a	n/a
47	CTCF	chr3:112930840-112930990	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr3:112933160-112933310	AG04449	skin:	n/a	n/a
49	CTCF	chr3:112930820-112930970	SAEC	small airway:	n/a	n/a
50	CTCF	chr3:112930840-112930990	Caco-2	colon:	n/a	n/a

(count:1589 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112935090-112935140	Jurkat	blood:	n/a
2	chr3:112927486-112927536	BE2_C	brain:	n/a
3	chr3:112899162-112899212	K562	blood:	n/a
4	chr3:112935090-112935140	Jurkat	blood:	n/a
5	chr3:112927486-112927536	BE2_C	brain:	n/a
6	chr3:112899162-112899212	K562	blood:	n/a
7	chr3:112931496-112931546	HRPEpiC	eye:	n/a
8	chr3:112931348-112931398	HIPEpiC	eye:	n/a
9	chr3:112935078-112935128	MCF10A-Er-Src	breast:	n/a
10	chr3:112893835-112893885	HCF	heart:	n/a
11	chr3:112934087-112934137	AG04450	lung:	fetal
12	chr3:112893835-112893885	HEK293	kidney:	embryo
13	chr3:112912841-112912891	HCF	heart:	n/a
14	chr3:112931202-112931252	HIPEpiC	eye:	n/a
15	chr3:112931354-112931404	SK-N-MC	brain:	n/a
16	chr3:112929830-112929880	HL-60	blood:	n/a
17	chr3:112931354-112931404	PFSK-1	brain:	n/a
18	chr3:112931496-112931546	SAEC	small airway:	n/a
19	chr3:112932345-112932395	HNPCEpiC	eye:	n/a
20	chr3:112931390-112931440	ECC-1	luminal epithelium:	n/a
21	chr3:112930675-112930725	ovcar-3	ovarian:	n/a
22	chr3:112932345-112932395	PANC-1	pancreas:	n/a
23	chr3:112930675-112930725	PANC-1	pancreas:	n/a
24	chr3:112932345-112932395	LNCaP	prostate:	n/a
25	chr3:112931354-112931404	HEK293	kidney:	embryo
26	chr3:112929672-112929722	HCF	heart:	n/a
27	chr3:112927486-112927536	NHBE	bronchial:	n/a
28	chr3:112930187-112930237	MCF-7	breast:	n/a
29	chr3:112927486-112927536	NH-A	brain:	n/a
30	chr3:112931354-112931404	HPAEpiC	pulmonary alveolar:	n/a
31	chr3:112934149-112934199	K562	blood:	n/a
32	chr3:112932345-112932395	A549	lung:	n/a
33	chr3:112930187-112930237	IMR90	lung:	fetal
34	chr3:112931348-112931398	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:112935078-112935128	NH-A	brain:	n/a
36	chr3:112931390-112931440	NB4	blood:	n/a
37	chr3:112932345-112932395	PrEC	prostate:	n/a
38	chr3:112931202-112931252	GM06990	blood:	n/a
39	chr3:112931348-112931398	T-47D	breast:	n/a
40	chr3:112931348-112931398	GM12878	blood:	n/a
41	chr3:112931202-112931252	AG04450	lung:	fetal
42	chr3:112927486-112927536	Jurkat	blood:	n/a
43	chr3:112931348-112931398	SK-N-SH	brain:	n/a
44	chr3:112934087-112934137	SK-N-SH_RA	brain:	n/a
45	chr3:112930675-112930725	BE2_C	brain:	n/a
46	chr3:112931202-112931252	HepG2	liver:	n/a
47	chr3:112931390-112931440	HMEC	breast:	n/a
48	chr3:112931496-112931546	HCT-116	colon:	n/a
49	chr3:112931390-112931440	K562	blood:	n/a
50	chr3:112931202-112931252	Jurkat	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:61735022..61735793-chr3:112930479..112931247,2	HCT-116	colon:
2	chr3:112915609..112917201-chr3:112917394..112919317,2	MCF-7	breast:
3	chr3:112898264..112901206-chr3:112912103..112913849,2	MCF-7	breast:
4	chr3:112903218..112904900-chr3:112913646..112916634,2	MCF-7	breast:
5	chr3:112929165..112932026-chr3:112933299..112935458,2	K562	blood:
6	chr3:112898328..112901487-chr3:112902253..112906214,3	MCF-7	breast:
7	chr3:112919722..112921654-chr3:112929649..112931314,2	MCF-7	breast:
8	chr3:112903218..112904900-chr3:112913646..112916634,2	MCF-7	breast:
9	chr3:112915609..112917201-chr3:112917394..112919317,2	MCF-7	breast:
10	chr3:112929722..112932026-chr3:112933958..112936481,2	K562	blood:
11	chr3:112875811..112877981-chr3:112929321..112930900,2	MCF-7	breast:
12	chr3:112898328..112901487-chr3:112902253..112906214,3	MCF-7	breast:
13	chr3:112933785..112936197-chr3:112937000..112939825,2	K562	blood:
14	chr3:112929722..112932026-chr3:112933958..112936481,2	K562	blood:
15	chr3:112929165..112932026-chr3:112933299..112935458,2	K562	blood:
16	chr3:112898264..112901206-chr3:112912103..112913849,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GTPBP8-1	chr3:112901899-112902095	NONHSAT091221
2	lnc-GTPBP8-1	chr3:112901900-112902148	ENSG00000240057.1
3	lnc-GTPBP8-1	chr3:112901900-112902095	XLOC_002760
4	lnc-BOC-1	chr3:112925260-112928430	ucscGeneNc_uc003dyb_1

No data

Variant related genes	Relation type
BOC	TF binding region
BOC	CpG island
ENSG00000167996	chromatin interactions
ENSG00000144857	chromatin interactions
ENSG00000269089	chromatin interactions
ENSG00000240057	chromatin interactions

Extended variants
information (count: 1628 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:1628 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6770031	chr3:112893640-112893641	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs192669410	chr3:112893646-112893647	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs6794383	chr3:112893653-112893654	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs568022019	chr3:112893685-112893686	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556256652	chr3:112893692-112893693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571281890	chr3:112893723-112893724	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs28431300	chr3:112893726-112893727	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553766279	chr3:112893776-112893777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs114187270	chr3:112893869-112893870	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs545537557	chr3:112893873-112893874	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs78387240	chr3:112893899-112893900	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs183736565	chr3:112893902-112893903	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs543666991	chr3:112893909-112893910	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs76727308	chr3:112893966-112893967	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs13320844	chr3:112893993-112893994	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs62264195	chr3:112893998-112893999	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs367571390	chr3:112894017-112894018	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs572244499	chr3:112894018-112894019	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs144470404	chr3:112894022-112894023	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs115375346	chr3:112894029-112894030	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs188059146	chr3:112894047-112894048	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs570231440	chr3:112894096-112894097	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs531152690	chr3:112894112-112894113	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs76541410	chr3:112894127-112894128	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs148434934	chr3:112894147-112894148	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs143721375	chr3:112894210-112894211	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs201968921	chr3:112894211-112894212	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs200422216	chr3:112894212-112894213	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs201420543	chr3:112894214-112894215	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs375972684	chr3:112894291-112894292	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs931700	chr3:112894315-112894316	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs565337779	chr3:112894322-112894323	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs62264196	chr3:112894339-112894340	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs370641266	chr3:112894359-112894360	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs931699	chr3:112894382-112894383	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs575803018	chr3:112894398-112894399	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs543231108	chr3:112894443-112894444	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs62264197	chr3:112894487-112894488	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs573850127	chr3:112894506-112894507	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
40	rs117394003	chr3:112894521-112894522	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
41	rs559744897	chr3:112894567-112894568	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs533381346	chr3:112894596-112894597	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs545492846	chr3:112894603-112894604	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs142904597	chr3:112894619-112894620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs531070693	chr3:112894652-112894653	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs549304436	chr3:112894697-112894698	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs111374012	chr3:112894713-112894714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541008449	chr3:112894752-112894753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs141402496	chr3:112894766-112894767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs62264198	chr3:112894776-112894777	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:61)

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
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Neurodevelopmental disorder	22521361	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	16608533	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Developmental delay	22180640	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Breast cancer	17142309	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	22174824	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ductal carcinoma	22052326	CNVD

Chromatin state (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112886400-112893800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr3:112886400-112893800	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr3:112889000-112896600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr3:112889200-112893800	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr3:112889200-112893800	Weak transcription	Fetal Stomach	stomach
6	chr3:112889200-112893800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr3:112889200-112898000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:112889400-112893800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr3:112889400-112894200	Weak transcription	Fetal Muscle Leg	muscle
10	chr3:112889400-112898200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr3:112892800-112893800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr3:112893000-112893800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:112893000-112894600	Enhancers	Colon Smooth Muscle	Colon
14	chr3:112893200-112894400	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr3:112893200-112894600	Enhancers	Fetal Lung	lung
16	chr3:112893200-112894600	Enhancers	Ovary	ovary
17	chr3:112893200-112894600	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr3:112893400-112894000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr3:112893400-112894400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr3:112893600-112894200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr3:112893600-112894600	Enhancers	Primary monocytes fromperipheralblood	blood
22	chr3:112893800-112894000	Enhancers	NHDF-Ad	bronchial
23	chr3:112893800-112894200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr3:112893800-112894400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr3:112893800-112894400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr3:112893800-112894400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr3:112893800-112894400	Enhancers	Stomach Smooth Muscle	stomach
28	chr3:112893800-112894600	Enhancers	H1 Cell Line	embryonic stem cell
29	chr3:112893800-112894600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr3:112893800-112894600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr3:112893800-112894600	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr3:112893800-112894600	Enhancers	Fetal Stomach	stomach
33	chr3:112893800-112894800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr3:112894000-112894200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr3:112894000-112894200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr3:112894000-112894200	Enhancers	Spleen	Spleen
37	chr3:112894000-112894600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr3:112894000-112894600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:112894200-112894600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr3:112894200-112894600	Enhancers	Fetal Muscle Leg	muscle
41	chr3:112894200-112898200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr3:112894200-112898400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr3:112894200-112898600	Weak transcription	Spleen	Spleen
44	chr3:112894200-112899200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr3:112894400-112896400	Weak transcription	Cortex derived primary cultured neurospheres	brain
46	chr3:112894400-112898400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
47	chr3:112894600-112895800	Weak transcription	Colon Smooth Muscle	Colon
48	chr3:112894600-112898600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr3:112894600-112899000	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr3:112894600-112899200	Weak transcription	H1 Cell Line	embryonic stem cell

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