Variant report

Variant	esv2830128
Chromosome Location	chr3:112090292-112144026
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:498)
CpG islands
(count:366)
Chromatin interactive
region (count:3)
LncRNA
region (count:15)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:498 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:112125881-112127134	GM12878	blood:	n/a	n/a
2	ATF2	chr3:112126396-112127097	GM12878	blood:	n/a	n/a
3	ATF2	chr3:112135258-112135975	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr3:112136351-112136756	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:112109999-112110295	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr3:112126731-112127049	GM12878	blood:	n/a	n/a
7	BATF	chr3:112125920-112126324	GM12878	blood:	n/a	n/a
8	BATF	chr3:112125953-112126291	GM12878	blood:	n/a	n/a
9	BCL11A	chr3:112124731-112124980	GM12878	blood:	n/a	n/a
10	BCL11A	chr3:112125955-112126331	GM12878	blood:	n/a	n/a
11	BCL11A	chr3:112125982-112126312	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:112126457-112127059	GM12878	blood:	n/a	n/a
13	BCL3	chr3:112096538-112096914	GM12878	blood:	n/a	n/a
14	BCL3	chr3:112132440-112132881	GM12878	blood:	n/a	n/a
15	BCL3	chr3:112100567-112100977	GM12878	blood:	n/a	n/a
16	BCL3	chr3:112126018-112126314	GM12878	blood:	n/a	n/a
17	BCL3	chr3:112126377-112127030	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:112124814-112124883	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:112125784-112127013	GM12878	blood:	n/a	n/a
20	BRCA1	chr3:112097204-112097414	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr3:112126984-112127210	HepG2	liver:	n/a	chr3:112127108-112127119
22	CEBPB	chr3:112097320-112097540	IMR90	lung:	n/a	n/a
23	CEBPB	chr3:112109597-112110853	Hela-S3	cervix:	n/a	chr3:112110019-112110027
24	CEBPB	chr3:112091213-112091523	A549	lung:	n/a	chr3:112091344-112091355
25	CEBPB	chr3:112127071-112127239	A549	lung:	n/a	chr3:112127108-112127119
26	CEBPB	chr3:112095783-112096092	A549	lung:	n/a	n/a
27	CEBPB	chr3:112091185-112091519	HepG2	liver:	n/a	chr3:112091344-112091355
28	CEBPB	chr3:112091255-112091521	IMR90	lung:	n/a	chr3:112091344-112091355
29	CEBPB	chr3:112127005-112127286	IMR90	lung:	n/a	chr3:112127108-112127119
30	CEBPB	chr3:112113085-112113329	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr3:112097151-112098213	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr3:112109678-112110897	IMR90	lung:	n/a	chr3:112110019-112110027
33	CEBPB	chr3:112097806-112098427	IMR90	lung:	n/a	n/a
34	CEBPB	chr3:112091163-112091578	Hela-S3	cervix:	n/a	chr3:112091344-112091355
35	CEBPB	chr3:112125534-112125626	HepG2	liver:	n/a	chr3:112125610-112125621
36	CEBPB	chr3:112095684-112096873	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr3:112093015-112093430	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr3:112095764-112096097	HepG2	liver:	n/a	n/a
39	CEBPB	chr3:112095724-112096413	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:112125791-112127014	GM12878	blood:	n/a	n/a
41	CHD1	chr3:112119873-112119968	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr3:112140127-112140197	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr3:112136553-112136625	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD1	chr3:112137058-112137137	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD1	chr3:112119127-112119148	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD1	chr3:112126750-112126937	GM12878	blood:	n/a	n/a
47	CHD2	chr3:112109914-112110297	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr3:112095801-112096284	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr3:112135332-112136391	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD2	chr3:112110187-112110508	Hela-S3	cervix:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:112113161-112113211	HUVEC	blood vessel:	n/a
2	chr3:112143970-112144020	K562	blood:	n/a
3	chr3:112109797-112109847	A549	lung:	n/a
4	chr3:112113161-112113211	HepG2	liver:	n/a
5	chr3:112117797-112117847	Jurkat	blood:	n/a
6	chr3:112096801-112096851	AG04449	skin:	fetal
7	chr3:112117797-112117847	ECC-1	luminal epithelium:	n/a
8	chr3:112113161-112113211	AG04450	lung:	fetal
9	chr3:112117797-112117847	GM06990	blood:	n/a
10	chr3:112143970-112144020	HRCEpiC	kidney:	n/a
11	chr3:112117797-112117847	PFSK-1	brain:	n/a
12	chr3:112117797-112117847	AG04449	skin:	fetal
13	chr3:112109797-112109847	PFSK-1	brain:	n/a
14	chr3:112109797-112109847	Hepatocyte	liver:	n/a
15	chr3:112096801-112096851	HepG2	liver:	n/a
16	chr3:112109797-112109847	GM19239	blood:	n/a
17	chr3:112113161-112113211	U87	brain:	n/a
18	chr3:112117797-112117847	IMR90	lung:	fetal
19	chr3:112096801-112096851	HUVEC	blood vessel:	n/a
20	chr3:112109797-112109847	HNPCEpiC	eye:	n/a
21	chr3:112117797-112117847	HUVEC	blood vessel:	n/a
22	chr3:112117797-112117847	SK-N-MC	brain:	n/a
23	chr3:112117797-112117847	HAEpiC	amniotic membrane:	n/a
24	chr3:112113161-112113211	BJ	skin:	n/a
25	chr3:112117797-112117847	Hela-S3	cervix:	n/a
26	chr3:112117797-112117847	HL-60	blood:	n/a
27	chr3:112143970-112144020	LNCaP	prostate:	n/a
28	chr3:112109797-112109847	GM06990	blood:	n/a
29	chr3:112113161-112113211	NHDF-neo	bronchial:	n/a
30	chr3:112143970-112144020	HL-60	blood:	n/a
31	chr3:112117797-112117847	GM12892	blood:	n/a
32	chr3:112117797-112117847	BE2_C	brain:	n/a
33	chr3:112096801-112096851	GM12891	blood:	n/a
34	chr3:112143970-112144020	HAEpiC	amniotic membrane:	n/a
35	chr3:112113161-112113211	Jurkat	blood:	n/a
36	chr3:112135991-112136041	LNCaP	prostate:	n/a
37	chr3:112143970-112144020	PrEC	prostate:	n/a
38	chr3:112113161-112113211	GM12892	blood:	n/a
39	chr3:112096801-112096851	ECC-1	luminal epithelium:	n/a
40	chr3:112135991-112136041	PFSK-1	brain:	n/a
41	chr3:112143970-112144020	AG04450	lung:	fetal
42	chr3:112117797-112117847	K562	blood:	n/a
43	chr3:112143970-112144020	T-47D	breast:	n/a
44	chr3:112117797-112117847	AG09319	gingival:	n/a
45	chr3:112117797-112117847	HCM	heart:	n/a
46	chr3:112135991-112136041	SKMC	muscle:	n/a
47	chr3:112143970-112144020	PFSK-1	brain:	n/a
48	chr3:112117797-112117847	MCF10A-Er-Src	breast:	n/a
49	chr3:112143970-112144020	NHBE	bronchial:	n/a
50	chr3:112135991-112136041	SK-N-SH	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:111832694..111835578-chr3:112096846..112099201,2	MCF-7	breast:
2	chr3:112090607..112092226-chr3:112097134..112099677,2	MCF-7	breast:
3	chr3:112090607..112092226-chr3:112097134..112099677,2	MCF-7	breast:

(count:15 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTLA-1	chr3:112123200-112123225	NONHSAT091170
2	lnc-BTLA-4	chr3:112130091-112130571	NONHSAT091178
3	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091174
4	lnc-BTLA-1	chr3:112100753-112100780	NONHSAT091174
5	lnc-BTLA-1	chr3:112099217-112099448	NONHSAT091176
6	lnc-BTLA-1	chr3:112115494-112116995	ENSG00000243081
7	lnc-BTLA-1	chr3:112100753-112100776	NONHSAT091168
8	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091172
9	lnc-BTLA-1	chr3:112127921-112128049	NONHSAT091169
10	lnc-BTLA-1	chr3:112099250-112099670	NONHSAT091173
11	lnc-BTLA-1	chr3:112100753-112100776	NONHSAT091176
12	lnc-BTLA-1	chr3:112127921-112127994	NONHSAT091172
13	lnc-BTLA-1	chr3:112127921-112127981	ENSG00000243081
14	lnc-BTLA-1	chr3:112099250-112099448	NONHSAT091168
15	lnc-BTLA-1	chr3:112127921-112127951	NONHSAT091167

No data

Variant related genes	Relation type
ENSG00000243081	TF binding region
ENSG00000243081	CpG island

Extended variants
information (count: 1991 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1991 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10934170	chr3:112090292-112090293	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs559655316	chr3:112090293-112090294	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs528527527	chr3:112090319-112090320	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs542094954	chr3:112090324-112090325	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs143561116	chr3:112090348-112090349	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530594935	chr3:112090351-112090352	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs75489455	chr3:112090412-112090413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563955192	chr3:112090472-112090473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs61550429	chr3:112090473-112090474	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs546380958	chr3:112090504-112090505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566453319	chr3:112090545-112090546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373106074	chr3:112090587-112090588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs548842664	chr3:112090623-112090624	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs555582677	chr3:112090625-112090626	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs113753407	chr3:112090646-112090647	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs375589029	chr3:112090673-112090674	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs537758485	chr3:112090701-112090702	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs543607983	chr3:112090727-112090728	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs577518580	chr3:112090730-112090731	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs539939037	chr3:112090761-112090762	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs371854415	chr3:112090801-112090802	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs140524663	chr3:112090824-112090825	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577454956	chr3:112090853-112090854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs57875359	chr3:112090907-112090908	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs193293884	chr3:112090925-112090926	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs575159774	chr3:112090976-112090977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs544109502	chr3:112090987-112090988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs541678957	chr3:112090989-112090990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1996723	chr3:112091001-112091002	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs60832135	chr3:112091013-112091014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150936281	chr3:112091031-112091032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs541706541	chr3:112091040-112091041	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546659657	chr3:112091041-112091042	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184743788	chr3:112091114-112091115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530072329	chr3:112091173-112091174	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548713036	chr3:112091198-112091199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs1996722	chr3:112091220-112091221	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs577588732	chr3:112091246-112091247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs188759372	chr3:112091274-112091275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs540540410	chr3:112091304-112091305	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs368589301	chr3:112091343-112091344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560798068	chr3:112091349-112091350	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114815567	chr3:112091366-112091367	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116540544	chr3:112091379-112091380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs60112764	chr3:112091460-112091461	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs368037939	chr3:112091483-112091484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539675970	chr3:112091492-112091493	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13080716	chr3:112091526-112091527	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs573227289	chr3:112091529-112091530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs116379211	chr3:112091597-112091598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Breast cancer	21858162	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Basal cell lymphoma	21115979	CNVD
Attention deficit hyperactivity disorder	22180640	CNVD
Breast cancer	22522925	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:112069200-112095400	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr3:112070800-112090600	Weak transcription	Brain Hippocampus Middle	brain
3	chr3:112077200-112094200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr3:112077600-112107200	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr3:112080000-112096000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr3:112081200-112092800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr3:112081400-112091600	Weak transcription	Primary T cells from cord blood	blood
8	chr3:112082200-112096000	Weak transcription	Fetal Stomach	stomach
9	chr3:112082600-112094600	Weak transcription	Brain Anterior Caudate	brain
10	chr3:112083400-112092200	Weak transcription	Primary B cells from cord blood	blood
11	chr3:112083800-112090600	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr3:112083800-112092200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
13	chr3:112084000-112090600	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr3:112084000-112094800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:112084200-112092600	Weak transcription	Fetal Kidney	kidney
16	chr3:112084400-112091600	Weak transcription	Placenta	Placenta
17	chr3:112084600-112093200	Weak transcription	Fetal Lung	lung
18	chr3:112084800-112096000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr3:112084800-112096800	Weak transcription	Fetal Muscle Leg	muscle
20	chr3:112085000-112095600	Weak transcription	Thymus	Thymus
21	chr3:112085400-112096000	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr3:112085600-112095400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr3:112085600-112096000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr3:112085800-112091400	Weak transcription	Primary B cells from peripheral blood	blood
25	chr3:112085800-112091400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr3:112085800-112091400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr3:112085800-112092200	Weak transcription	Primary hematopoietic stem cells	blood
28	chr3:112085800-112096400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr3:112085800-112096600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr3:112085800-112101400	Weak transcription	Aorta	Aorta
31	chr3:112086000-112095000	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr3:112086000-112095600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:112086200-112091200	Weak transcription	Brain Angular Gyrus	brain
34	chr3:112086200-112091400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:112086200-112092200	Weak transcription	Fetal Thymus	thymus
36	chr3:112087600-112096400	Weak transcription	HUES64 Cell Line	embryonic stem cell
37	chr3:112088000-112090600	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr3:112088200-112092800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr3:112088400-112091400	Weak transcription	Adipose Nuclei	Adipose
40	chr3:112090200-112090400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
41	chr3:112090400-112092600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr3:112090600-112090800	Flanking Active TSS	Sigmoid Colon	Sigmoid Colon
43	chr3:112090600-112093000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr3:112090600-112093600	Enhancers	Primary monocytes fromperipheralblood	blood
45	chr3:112090800-112091600	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr3:112091200-112092800	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr3:112091400-112091600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr3:112091400-112091600	Enhancers	Primary B cells from peripheral blood	blood
49	chr3:112091400-112091600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr3:112091400-112091600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links