Variant report

Variant	nsv1009634
Chromosome Location	chr3:134543259-134820208
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1524)
CpG islands
(count:671)
Chromatin interactive
region (count:25)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1524 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr3:134737365-134737784	GM12878	blood:	n/a	n/a
2	ATF2	chr3:134604740-134605325	GM12878	blood:	n/a	n/a
3	ATF2	chr3:134637252-134637641	GM12878	blood:	n/a	n/a
4	ATF2	chr3:134675181-134675695	GM12878	blood:	n/a	n/a
5	ATF2	chr3:134622890-134623728	GM12878	blood:	n/a	n/a
6	ATF2	chr3:134571661-134572256	GM12878	blood:	n/a	n/a
7	ATF2	chr3:134622961-134623647	GM12878	blood:	n/a	n/a
8	BACH1	chr3:134604707-134605103	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr3:134786215-134786398	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr3:134604732-134605140	GM12878	blood:	n/a	n/a
11	BATF	chr3:134648858-134649270	GM12878	blood:	n/a	n/a
12	BATF	chr3:134675322-134675601	GM12878	blood:	n/a	n/a
13	BATF	chr3:134593980-134594251	GM12878	blood:	n/a	n/a
14	BATF	chr3:134637299-134637631	GM12878	blood:	n/a	n/a
15	BATF	chr3:134593872-134594316	GM12878	blood:	n/a	n/a
16	BATF	chr3:134648898-134649220	GM12878	blood:	n/a	n/a
17	BATF	chr3:134623079-134623609	GM12878	blood:	n/a	chr3:134623596-134623605
18	BATF	chr3:134623791-134624062	GM12878	blood:	n/a	chr3:134623901-134623912
19	BATF	chr3:134623147-134623557	GM12878	blood:	n/a	n/a
20	BATF	chr3:134558078-134558261	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:134737385-134737727	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:134622653-134622911	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:134604745-134605115	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:134622984-134623516	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:134622912-134623583	GM12878	blood:	n/a	chr3:134623549-134623558
26	BCL11A	chr3:134571788-134572158	GM12878	blood:	n/a	n/a
27	BCL3	chr3:134623125-134623593	GM12878	blood:	n/a	chr3:134623549-134623558
28	BCL3	chr3:134571745-134572156	GM12878	blood:	n/a	n/a
29	BCL3	chr3:134623052-134623464	GM12878	blood:	n/a	n/a
30	BCLAF1	chr3:134571640-134572229	GM12878	blood:	n/a	n/a
31	BCLAF1	chr3:134622885-134623710	GM12878	blood:	n/a	chr3:134623549-134623558
32	BCLAF1	chr3:134571655-134572257	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:134622940-134623634	GM12878	blood:	n/a	chr3:134623549-134623558
34	BHLHE40	chr3:134737060-134737736	GM12878	blood:	n/a	n/a
35	BHLHE40	chr3:134742787-134743472	GM12878	blood:	n/a	n/a
36	BHLHE40	chr3:134675049-134675590	GM12878	blood:	n/a	chr3:134675339-134675348 chr3:134675339-134675348 chr3:134675338-134675347
37	BHLHE40	chr3:134604658-134605348	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:134596783-134596859	HepG2	liver:	n/a	n/a
39	BHLHE40	chr3:134637280-134637682	GM12878	blood:	n/a	n/a
40	BHLHE40	chr3:134571626-134572252	GM12878	blood:	n/a	n/a
41	BHLHE40	chr3:134622655-134624067	GM12878	blood:	n/a	n/a
42	BHLHE40	chr3:134576305-134576527	GM12878	blood:	n/a	n/a
43	BHLHE40	chr3:134598925-134599195	HepG2	liver:	n/a	n/a
44	BRCA1	chr3:134736236-134736333	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr3:134565829-134565857	GM12878	blood:	n/a	n/a
46	CEBPB	chr3:134656549-134657159	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr3:134772757-134772802	HepG2	liver:	n/a	chr3:134772784-134772795
48	CEBPB	chr3:134615615-134615968	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr3:134615614-134615959	HepG2	liver:	n/a	n/a
50	CEBPB	chr3:134569748-134569855	HepG2	liver:	n/a	chr3:134569792-134569803

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:134801915-134801965	ovcar-3	ovarian:	n/a
2	chr3:134801915-134801965	H1-hESC	embryonic stem cell:	embryo
3	chr3:134635261-134635311	HAEpiC	amniotic membrane:	n/a
4	chr3:134634602-134634652	HUVEC	blood vessel:	n/a
5	chr3:134611847-134611897	GM12878	blood:	n/a
6	chr3:134758333-134758383	NB4	blood:	n/a
7	chr3:134758333-134758383	GM12891	blood:	n/a
8	chr3:134710864-134710914	HUVEC	blood vessel:	n/a
9	chr3:134798947-134798997	PANC-1	pancreas:	n/a
10	chr3:134656829-134656879	HRPEpiC	eye:	n/a
11	chr3:134819027-134819077	HCT-116	colon:	n/a
12	chr3:134798947-134798997	Hepatocyte	liver:	n/a
13	chr3:134798947-134798997	AG04450	lung:	fetal
14	chr3:134656829-134656879	Hela-S3	cervix:	n/a
15	chr3:134710864-134710914	IMR90	lung:	fetal
16	chr3:134798947-134798997	Hela-S3	cervix:	n/a
17	chr3:134819027-134819077	SKMC	muscle:	n/a
18	chr3:134798947-134798997	HUVEC	blood vessel:	n/a
19	chr3:134649578-134649628	U87	brain:	n/a
20	chr3:134635534-134635584	PFSK-1	brain:	n/a
21	chr3:134635261-134635311	RPTEC	kidney:	n/a
22	chr3:134635261-134635311	PrEC	prostate:	n/a
23	chr3:134635261-134635311	SKMC	muscle:	n/a
24	chr3:134710864-134710914	HRPEpiC	eye:	n/a
25	chr3:134635534-134635584	HCT-116	colon:	n/a
26	chr3:134634602-134634652	GM12878	blood:	n/a
27	chr3:134819027-134819077	HCM	heart:	n/a
28	chr3:134656829-134656879	H1-hESC	embryonic stem cell:	embryo
29	chr3:134656829-134656879	SK-N-SH_RA	brain:	n/a
30	chr3:134611847-134611897	HepG2	liver:	n/a
31	chr3:134819027-134819077	SK-N-MC	brain:	n/a
32	chr3:134710864-134710914	AG09319	gingival:	n/a
33	chr3:134798947-134798997	MCF-7	breast:	n/a
34	chr3:134611847-134611897	HCF	heart:	n/a
35	chr3:134635261-134635311	HL-60	blood:	n/a
36	chr3:134656829-134656879	GM19239	blood:	n/a
37	chr3:134634602-134634652	ovcar-3	ovarian:	n/a
38	chr3:134656829-134656879	CMK	blood:	n/a
39	chr3:134649578-134649628	PFSK-1	brain:	n/a
40	chr3:134611847-134611897	ProgFib	skin:	n/a
41	chr3:134656829-134656879	PrEC	prostate:	n/a
42	chr3:134710864-134710914	Caco-2	colon:	n/a
43	chr3:134634602-134634652	CMK	blood:	n/a
44	chr3:134635534-134635584	ovcar-3	ovarian:	n/a
45	chr3:134656829-134656879	NHDF-neo	bronchial:	n/a
46	chr3:134798947-134798997	MCF10A-Er-Src	breast:	n/a
47	chr3:134611847-134611897	AG04449	skin:	fetal
48	chr3:134758333-134758383	AG09309	skin:	n/a
49	chr3:134758333-134758383	MCF-7	breast:	n/a
50	chr3:134635261-134635311	HCM	heart:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:134769674..134771857-chr3:134772148..134774562,2	K562	blood:
2	chr3:134667860..134670173-chr3:134674253..134676895,2	K562	blood:
3	chr3:134711495..134714035-chr3:134895700..134897544,2	K562	blood:
4	chr3:134669641..134672133-chr3:134679673..134681914,2	K562	blood:
5	chr3:134725899..134728503-chr3:134730689..134733347,3	MCF-7	breast:
6	chr3:134769674..134771857-chr3:134772148..134774562,2	K562	blood:
7	chr3:134640278..134641872-chr3:134645739..134647290,2	K562	blood:
8	chr3:134562864..134564396-chr3:134566053..134568096,2	K562	blood:
9	chr3:134670207..134673023-chr3:134688821..134691750,2	MCF-7	breast:
10	chr3:134640278..134641872-chr3:134645739..134647290,2	K562	blood:
11	chr3:134550436..134552836-chr3:134565260..134567786,2	K562	blood:
12	chr3:134606424..134609359-chr3:134641100..134643520,2	K562	blood:
13	chr3:134667860..134670173-chr3:134674253..134676895,2	K562	blood:
14	chr3:134550436..134552836-chr3:134565260..134567786,2	K562	blood:
15	chr3:134585220..134586106-chr6:69710636..69711412,2	MCF-7	breast:
16	chr3:134562864..134564396-chr3:134566053..134568096,2	K562	blood:
17	chr3:134513827..134514378-chr3:134719808..134720327,2	MCF-7	breast:
18	chr14:88237611..88238152-chr3:134576314..134576834,2	MCF-7	breast:
19	chr3:134669641..134672133-chr3:134679673..134681914,2	K562	blood:
20	chr3:134725899..134728503-chr3:134730689..134733347,3	MCF-7	breast:
21	chr3:134795759..134797342-chr3:134802255..134804359,2	MCF-7	breast:
22	chr3:134606424..134609359-chr3:134641100..134643520,2	K562	blood:
23	chr3:134670207..134673023-chr3:134688821..134691750,2	MCF-7	breast:
24	chr3:134814726..134816547-chr3:134832650..134834181,2	K562	blood:
25	chr3:134795759..134797342-chr3:134802255..134804359,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KY-6	chr3:134650315-134650429	ucscGeneNc_uc003epo_2
2	lnc-KY-6	chr3:134646939-134647109	ucscGeneNc_uc003epo_2
3	lnc-KY-5	chr3:134570598-134571412	NONHSAT092256
4	lnc-KY-6	chr3:134630821-134631243	ucscGeneNc_uc003epo_2
5	lnc-KY-5	chr3:134572318-134572589	NONHSAT092256
6	lnc-KY-6	chr3:134656863-134656997	ucscGeneNc_uc003epo_2
7	lnc-KY-5	chr3:134573241-134573341	NONHSAT092256
8	lnc-KY-6	chr3:134657279-134657310	ucscGeneNc_uc003epo_2
9	lnc-KY-5	chr3:134572033-134572222	NONHSAT092256

No data

Variant related genes	Relation type
EPHB1	TF binding region
EPHB1	CpG island
ENSG00000154928	chromatin interactions

Extended variants
information (count: 10487 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:10487 , 50 per page) page: 1 2 3 4 5 6 7 ... 210

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs116011323	chr3:134543261-134543262	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73229116	chr3:134543393-134543394	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs573368020	chr3:134543404-134543405	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs62272413	chr3:134543416-134543417	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs76828326	chr3:134543449-134543450	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs373285670	chr3:134543452-134543453	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112423534	chr3:134543455-134543456	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543319168	chr3:134543488-134543489	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs376814770	chr3:134543560-134543561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557244107	chr3:134543565-134543566	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs576382901	chr3:134543585-134543586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545403697	chr3:134543611-134543612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs62272414	chr3:134543626-134543627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs138115893	chr3:134543659-134543660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs7611548	chr3:134543701-134543702	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs541935491	chr3:134543742-134543743	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs532227128	chr3:134543763-134543764	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs73229119	chr3:134543777-134543778	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs531149993	chr3:134543778-134543779	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550961272	chr3:134543869-134543870	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs543974205	chr3:134543891-134543892	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180729469	chr3:134543919-134543920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs7611739	chr3:134543923-134543924	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs547016038	chr3:134543924-134543925	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs7633831	chr3:134543925-134543926	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7633835	chr3:134543935-134543936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370195263	chr3:134543949-134543950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs555845904	chr3:134543956-134543957	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs568134341	chr3:134543972-134543973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142821389	chr3:134543980-134543981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556937111	chr3:134544000-134544001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7634094	chr3:134544022-134544023	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs367634036	chr3:134544049-134544050	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7645705	chr3:134544061-134544062	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs186085905	chr3:134544074-134544075	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs572537676	chr3:134544084-134544085	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541523907	chr3:134544089-134544090	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs376696445	chr3:134544094-134544095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs141179867	chr3:134544095-134544096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs192192057	chr3:134544127-134544128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs530959044	chr3:134544142-134544143	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544785589	chr3:134544178-134544179	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs369558455	chr3:134544197-134544198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs145060821	chr3:134544204-134544205	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs533648125	chr3:134544245-134544246	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs183443119	chr3:134544264-134544265	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73229122	chr3:134544282-134544283	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs6802089	chr3:134544299-134544300	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs6789449	chr3:134544322-134544323	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs185830721	chr3:134544329-134544330	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	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
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
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
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD
Autism	21865298	CNVD

Chromatin state (count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:134529600-134546400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr3:134534800-134546000	Weak transcription	Right Atrium	heart
3	chr3:134537000-134543400	Weak transcription	Psoas Muscle	Psoas
4	chr3:134537800-134545600	Weak transcription	GM12878-XiMat	blood
5	chr3:134540600-134544600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr3:134541000-134543600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr3:134541200-134547400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr3:134543000-134544400	Enhancers	Skeletal Muscle Male	skeletal muscle
9	chr3:134543200-134544000	Enhancers	Fetal Brain Female	brain
10	chr3:134543200-134544200	Enhancers	Fetal Muscle Leg	muscle
11	chr3:134543400-134544400	Enhancers	Psoas Muscle	Psoas
12	chr3:134543600-134543800	Enhancers	Fetal Brain Male	brain
13	chr3:134543600-134544400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:134543800-134546000	Weak transcription	Fetal Brain Male	brain
15	chr3:134544000-134546800	Weak transcription	Fetal Brain Female	brain
16	chr3:134544400-134546200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr3:134544600-134545600	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr3:134545600-134546000	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chr3:134545600-134547600	Enhancers	GM12878-XiMat	blood
20	chr3:134546000-134549800	Enhancers	Fetal Brain Male	brain
21	chr3:134546000-134558000	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr3:134546200-134546800	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr3:134546600-134546800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
24	chr3:134546600-134547000	Enhancers	Brain Anterior Caudate	brain
25	chr3:134546800-134547600	Enhancers	Fetal Brain Female	brain
26	chr3:134546800-134548800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr3:134547000-134547400	Weak transcription	Brain Anterior Caudate	brain
28	chr3:134547400-134547600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr3:134547400-134547600	Enhancers	Brain Anterior Caudate	brain
30	chr3:134547600-134548600	Weak transcription	Fetal Brain Female	brain
31	chr3:134547600-134550400	Weak transcription	Brain Anterior Caudate	brain
32	chr3:134547600-134551000	Weak transcription	GM12878-XiMat	blood
33	chr3:134548600-134549600	Enhancers	Fetal Brain Female	brain
34	chr3:134548800-134549000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr3:134549000-134549400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr3:134549400-134549600	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr3:134549600-134550200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr3:134549600-134554400	Weak transcription	Fetal Brain Female	brain
39	chr3:134549800-134551000	Enhancers	Brain Hippocampus Middle	brain
40	chr3:134549800-134551200	Enhancers	Brain Angular Gyrus	brain
41	chr3:134549800-134551200	Enhancers	Brain Cingulate Gyrus	brain
42	chr3:134549800-134551400	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr3:134549800-134569400	Weak transcription	Fetal Brain Male	brain
44	chr3:134550000-134551200	Enhancers	Brain Substantia Nigra	brain
45	chr3:134550200-134550600	Enhancers	Breast Myoepithelial Primary Cells	Breast
46	chr3:134550400-134551400	Enhancers	Brain Anterior Caudate	brain
47	chr3:134550600-134552000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
48	chr3:134551000-134553600	Enhancers	GM12878-XiMat	blood
49	chr3:134552000-134553000	Enhancers	Breast Myoepithelial Primary Cells	Breast
50	chr3:134552400-134552800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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