Variant report

Variant	nsv869920
Chromosome Location	chr3:100336028-100437968
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1731)
CpG islands
(count:1223)
Chromatin interactive
region (count:66)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1731 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:100369723-100370159	K562	blood:	n/a	n/a
2	ARID3A	chr3:100353734-100354533	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:100428405-100428550	K562	blood:	n/a	n/a
4	ARID3A	chr3:100427756-100428585	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:100381238-100381404	K562	blood:	n/a	n/a
6	ARID3A	chr3:100400484-100400645	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:100359648-100359874	HepG2	liver:	n/a	n/a
8	ARID3A	chr3:100348388-100349223	K562	blood:	n/a	n/a
9	ARID3A	chr3:100353731-100353930	K562	blood:	n/a	n/a
10	ATF1	chr3:100427978-100428440	K562	blood:	n/a	n/a
11	ATF1	chr3:100353718-100353993	K562	blood:	n/a	n/a
12	ATF1	chr3:100348373-100348950	K562	blood:	n/a	n/a
13	ATF2	chr3:100427777-100428567	GM12878	blood:	n/a	n/a
14	ATF2	chr3:100429275-100429952	GM12878	blood:	n/a	n/a
15	ATF2	chr3:100360476-100360923	GM12878	blood:	n/a	n/a
16	ATF2	chr3:100369506-100370238	GM12878	blood:	n/a	n/a
17	ATF3	chr3:100348592-100348961	K562	blood:	n/a	n/a
18	ATF3	chr3:100370050-100370425	K562	blood:	n/a	n/a
19	BACH1	chr3:100428023-100428678	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr3:100381410-100381594	K562	blood:	n/a	n/a
21	BACH1	chr3:100349457-100349877	H1-hESC	embryonic stem cell:	n/a	chr3:100349697-100349711
22	BACH1	chr3:100421452-100421833	K562	blood:	n/a	n/a
23	BACH1	chr3:100421524-100421801	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr3:100369687-100370030	GM12878	blood:	n/a	n/a
25	BATF	chr3:100429333-100429812	GM12878	blood:	n/a	n/a
26	BATF	chr3:100369685-100370004	GM12878	blood:	n/a	n/a
27	BATF	chr3:100429220-100429801	GM12878	blood:	n/a	n/a
28	BATF	chr3:100360240-100360471	GM12878	blood:	n/a	n/a
29	BATF	chr3:100360218-100360885	GM12878	blood:	n/a	chr3:100360555-100360566
30	BCL11A	chr3:100360611-100360835	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:100360195-100360894	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:100360235-100360494	GM12878	blood:	n/a	n/a
33	BCLAF1	chr3:100429350-100429879	GM12878	blood:	n/a	chr3:100429694-100429703 chr3:100429744-100429753 chr3:100429743-100429752
34	BCLAF1	chr3:100428169-100428667	GM12878	blood:	n/a	chr3:100428545-100428558 chr3:100428541-100428554 chr3:100428539-100428552
35	BHLHE40	chr3:100428011-100428266	A549	lung:	n/a	n/a
36	BHLHE40	chr3:100353686-100354022	GM12878	blood:	n/a	n/a
37	BHLHE40	chr3:100369647-100370331	GM12878	blood:	n/a	n/a
38	BHLHE40	chr3:100428885-100428960	K562	blood:	n/a	n/a
39	BHLHE40	chr3:100353728-100354019	HepG2	liver:	n/a	n/a
40	BHLHE40	chr3:100427970-100428628	HepG2	liver:	n/a	chr3:100428533-100428549
41	BHLHE40	chr3:100427985-100428525	K562	blood:	n/a	n/a
42	BHLHE40	chr3:100353702-100354034	K562	blood:	n/a	n/a
43	BHLHE40	chr3:100427893-100428554	GM12878	blood:	n/a	chr3:100428533-100428549
44	BHLHE40	chr3:100360142-100360910	GM12878	blood:	n/a	n/a
45	BRCA1	chr3:100427676-100428558	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr3:100428290-100428586	HepG2	liver:	n/a	n/a
47	BRCA1	chr3:100427866-100428531	GM12878	blood:	n/a	n/a
48	BRCA1	chr3:100428898-100429175	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr3:100427800-100428582	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr3:100429415-100429752	Hela-S3	cervix:	n/a	n/a

(count:1223 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:100428398-100428448	HCPEpiC	choroid plexus:	n/a
2	chr3:100428070-100428120	BJ	skin:	n/a
3	chr3:100428869-100428919	SK-N-SH_RA	brain:	n/a
4	chr3:100428398-100428448	HCPEpiC	choroid plexus:	n/a
5	chr3:100428070-100428120	BJ	skin:	n/a
6	chr3:100428869-100428919	SK-N-SH_RA	brain:	n/a
7	chr3:100424830-100424880	GM06990	blood:	n/a
8	chr3:100437347-100437397	ProgFib	skin:	n/a
9	chr3:100428005-100428055	MCF10A-Er-Src	breast:	n/a
10	chr3:100401270-100401320	Hepatocyte	liver:	n/a
11	chr3:100428172-100428222	HCF	heart:	n/a
12	chr3:100428172-100428222	SK-N-SH	brain:	n/a
13	chr3:100428642-100428692	HRPEpiC	eye:	n/a
14	chr3:100428172-100428222	AG04449	skin:	fetal
15	chr3:100437347-100437397	AG09309	skin:	n/a
16	chr3:100428869-100428919	HAEpiC	amniotic membrane:	n/a
17	chr3:100428005-100428055	NT2-D1	testis:	n/a
18	chr3:100428145-100428195	PrEC	prostate:	n/a
19	chr3:100437347-100437397	NH-A	brain:	n/a
20	chr3:100424830-100424880	BE2_C	brain:	n/a
21	chr3:100428140-100428190	GM12892	blood:	n/a
22	chr3:100430811-100430861	HepG2	liver:	n/a
23	chr3:100428140-100428190	AG04449	skin:	fetal
24	chr3:100349374-100349424	BE2_C	brain:	n/a
25	chr3:100430811-100430861	HEK293	kidney:	embryo
26	chr3:100428033-100428083	SK-N-MC	brain:	n/a
27	chr3:100427096-100427146	AG10803	skin:	n/a
28	chr3:100401284-100401334	HNPCEpiC	eye:	n/a
29	chr3:100428869-100428919	SKMC	muscle:	n/a
30	chr3:100437347-100437397	ECC-1	luminal epithelium:	n/a
31	chr3:100424830-100424880	PANC-1	pancreas:	n/a
32	chr3:100428147-100428197	HCT-116	colon:	n/a
33	chr3:100428145-100428195	ovcar-3	ovarian:	n/a
34	chr3:100428005-100428055	AoSMC	blood vessel:	n/a
35	chr3:100428140-100428190	Caco-2	colon:	n/a
36	chr3:100401284-100401334	NHDF-neo	bronchial:	n/a
37	chr3:100428140-100428190	NHDF-neo	bronchial:	n/a
38	chr3:100428642-100428692	GM12892	blood:	n/a
39	chr3:100429064-100429114	AG10803	skin:	n/a
40	chr3:100429064-100429114	SKMC	muscle:	n/a
41	chr3:100428005-100428055	HCM	heart:	n/a
42	chr3:100428145-100428195	H1-hESC	embryonic stem cell:	embryo
43	chr3:100428642-100428692	BJ	skin:	n/a
44	chr3:100401284-100401334	PFSK-1	brain:	n/a
45	chr3:100428172-100428222	PrEC	prostate:	n/a
46	chr3:100428140-100428190	T-47D	breast:	n/a
47	chr3:100424830-100424880	HIPEpiC	eye:	n/a
48	chr3:100428070-100428120	RPTEC	kidney:	n/a
49	chr3:100428172-100428222	AG04450	lung:	fetal
50	chr3:100428033-100428083	AoSMC	blood vessel:	n/a

(count:66 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:100120818..100123698-chr3:100370041..100372201,2	K562	blood:
2	chr3:100321003..100323549-chr3:100347554..100350487,3	MCF-7	breast:
3	chr17:57918588..57920867-chr3:100426772..100429347,2	MCF-7	breast:
4	chr3:100428169..100430169-chr3:100436770..100441506,6	MCF-7	breast:
5	chr3:100181153..100182757-chr3:100352927..100354311,7	MCF-7	breast:
6	chr3:100421148..100423017-chr3:100443429..100446212,2	K562	blood:
7	chr3:100425991..100429784-chr3:100429994..100431694,4	K562	blood:
8	chr3:100348848..100350778-chr3:100351417..100355406,3	K562	blood:
9	chr3:100420077..100423053-chr3:100428087..100429810,2	MCF-7	breast:
10	chr1:151512640..151513443-chr3:100428519..100429048,2	Hela-S3	cervix:
11	chr3:100321992..100322818-chr3:100353419..100354308,2	MCF-7	breast:
12	chr3:100325407..100326196-chr3:100353394..100354270,2	MCF-7	breast:
13	chr3:100353552..100356244-chr3:100358458..100360777,2	K562	blood:
14	chr3:100419966..100423130-chr3:100426813..100428964,3	K562	blood:
15	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
16	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
17	chr3:100412000..100414603-chr3:100428096..100429901,2	K562	blood:
18	chr3:100279818..100281392-chr3:100419411..100421780,2	K562	blood:
19	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
20	chr3:100118702..100121299-chr3:100427057..100432444,4	K562	blood:
21	chr3:100348848..100350394-chr3:100351417..100354134,2	K562	blood:
22	chr3:100325886..100329093-chr3:100426560..100431642,4	MCF-7	breast:
23	chr18:3247419..3248282-chr3:100427656..100428171,2	Hela-S3	cervix:
24	chr3:100322114..100322780-chr3:100353316..100353989,3	MCF-7	breast:
25	chr3:99535346..99537040-chr3:100436340..100438429,2	K562	blood:
26	chr3:100414154..100421316-chr3:100422241..100429195,9	MCF-7	breast:
27	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
28	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
29	chr3:100427232..100427732-chr9:96215167..96215670,2	Hela-S3	cervix:
30	chr1:73273811..73275334-chr3:100425817..100428133,2	MCF-7	breast:
31	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
32	chr3:100325466..100327241-chr3:100349090..100350621,2	K562	blood:
33	chr3:100410212..100413199-chr3:100413505..100415346,2	K562	blood:
34	chr2:67550820..67551820-chr3:100427957..100428561,3	HCT-116	colon:
35	chr3:100419538..100421699-chr3:100430283..100434420,3	MCF-7	breast:
36	chr3:100428095..100432338-chr3:100432996..100435628,5	K562	blood:
37	chr3:100374838..100376761-chr3:100378684..100380359,2	K562	blood:
38	chr3:100428105..100429880-chr3:100429992..100431694,2	K562	blood:
39	chr3:100367436..100369530-chr3:100426605..100429472,2	MCF-7	breast:
40	chr20:33543190..33544135-chr3:100427443..100428252,2	NB4	blood:
41	chr3:100432153..100434876-chr3:100437236..100438974,2	MCF-7	breast:
42	chr3:100372478..100376338-chr3:100378859..100382078,3	K562	blood:
43	chr3:100340717..100343040-chr3:100348395..100351881,3	K562	blood:
44	chr3:100417750..100419779-chr3:100427601..100429655,2	K562	blood:
45	chr3:100369607..100371401-chr3:100374454..100376110,2	K562	blood:
46	chr3:100412832..100415800-chr3:100417725..100420372,2	K562	blood:
47	chr3:100355413..100357441-chr3:100427541..100429664,2	K562	blood:
48	chr3:100432846..100436544-chr3:100436912..100439975,5	K562	blood:
49	chr3:100415596..100419109-chr3:100421112..100424187,4	K562	blood:
50	chr3:100358087..100360713-chr3:100362813..100364716,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABI3BP-1	chr3:100383894-100384320	NONHSAT090876
2	lnc-TMEM45A-1	chr3:100356146-100356419	NONHSAT090874
3	lnc-TMEM45A-1	chr3:100354384-100354670	NONHSAT090874

No data

Variant related genes	Relation type
TFG	TF binding region
GPR128	TF binding region
ENSG00000252989	TF binding region
GMFBP1	TF binding region
TFG	CpG island
GPR128	CpG island
ENSG00000252989	CpG island
GMFBP1	CpG island
ENSG00000154174	chromatin interactions
ENSG00000206535	chromatin interactions
ENSG00000232536	chromatin interactions
ENSG00000188938	chromatin interactions
ENSG00000100983	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000197728	chromatin interactions
ENSG00000166889	chromatin interactions
ENSG00000236605	chromatin interactions
ENSG00000144820	chromatin interactions
ENSG00000101608	chromatin interactions
ENSG00000143367	chromatin interactions
ENSG00000257449	chromatin interactions
ENSG00000114354	chromatin interactions
ENSG00000252989	chromatin interactions
ENSG00000184220	chromatin interactions

Extended variants
information (count: 4091 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4091 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553012720	chr3:100336076-100336077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574635783	chr3:100336077-100336078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs541856837	chr3:100336096-100336097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs563732392	chr3:100336097-100336098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs548126378	chr3:100336098-100336099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs543969902	chr3:100336130-100336131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs372953578	chr3:100336163-100336164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs143794036	chr3:100336215-100336216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs564644379	chr3:100336254-100336255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs528646424	chr3:100336291-100336292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs603630	chr3:100336306-100336307	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs181908097	chr3:100336309-100336310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs547570452	chr3:100336310-100336311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs529861377	chr3:100336361-100336362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368200265	chr3:100336372-100336373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs186446812	chr3:100336460-100336461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs569600486	chr3:100336477-100336478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536670540	chr3:100336486-100336487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs558769876	chr3:100336494-100336495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74473858	chr3:100336495-100336496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530097700	chr3:100336507-100336508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552797824	chr3:100336508-100336509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574572996	chr3:100336511-100336512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs542345311	chr3:100336521-100336522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557188353	chr3:100336540-100336541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs575564719	chr3:100336573-100336574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs545878215	chr3:100336590-100336591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564729823	chr3:100336591-100336592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs528834782	chr3:100336599-100336600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376032821	chr3:100336666-100336667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540826340	chr3:100336704-100336705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562294286	chr3:100336716-100336717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs529480371	chr3:100336732-100336733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190477868	chr3:100336738-100336739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs569655055	chr3:100336745-100336746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530484947	chr3:100336780-100336781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs551929855	chr3:100336821-100336822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs6770367	chr3:100336822-100336823	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs534632151	chr3:100336830-100336831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537752693	chr3:100336837-100336838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567878321	chr3:100336848-100336849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs372480641	chr3:100336862-100336863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs535309801	chr3:100336880-100336881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs139246943	chr3:100336886-100336887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6441367	chr3:100336889-100336890	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6783996	chr3:100336891-100336892	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs558229674	chr3:100336920-100336921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573554653	chr3:100336929-100336930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs540961210	chr3:100336982-100336983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562391578	chr3:100336989-100336990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	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
small cell lung cancer	20016488	CNVD
Ductal carcinoma	22052326	CNVD
Myelofibrosis	22110671	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21785460	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD

Chromatin state (count:1543 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:100334800-100339400	Weak transcription	Duodenum Mucosa	Duodenum
2	chr3:100334800-100339600	Weak transcription	Small Intestine	intestine
3	chr3:100335800-100339400	Weak transcription	Fetal Intestine Large	intestine
4	chr3:100335800-100339400	Weak transcription	Fetal Intestine Small	intestine
5	chr3:100339400-100339600	Enhancers	Sigmoid Colon	Sigmoid Colon
6	chr3:100339400-100339800	Enhancers	Fetal Intestine Large	intestine
7	chr3:100339400-100340000	Enhancers	Fetal Intestine Small	intestine
8	chr3:100339400-100340400	Enhancers	Duodenum Mucosa	Duodenum
9	chr3:100339600-100340800	Enhancers	Small Intestine	intestine
10	chr3:100339800-100343000	Weak transcription	Fetal Intestine Large	intestine
11	chr3:100340000-100341800	Weak transcription	Fetal Intestine Small	intestine
12	chr3:100340800-100341000	Weak transcription	Small Intestine	intestine
13	chr3:100340800-100341200	Enhancers	K562	blood
14	chr3:100341800-100342000	ZNF genes & repeats	Fetal Intestine Small	intestine
15	chr3:100343800-100352000	Weak transcription	Fetal Intestine Large	intestine
16	chr3:100346200-100348000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr3:100346400-100348200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr3:100347400-100347600	Enhancers	Small Intestine	intestine
19	chr3:100347400-100348600	Enhancers	Primary hematopoietic stem cells	blood
20	chr3:100347600-100349200	Weak transcription	Small Intestine	intestine
21	chr3:100347600-100350000	Enhancers	HUVEC	blood vessel
22	chr3:100347600-100350400	Enhancers	K562	blood
23	chr3:100347800-100349800	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr3:100348000-100348800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:100348200-100348600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr3:100348200-100349800	Enhancers	NHEK	skin
27	chr3:100348200-100352200	Weak transcription	Primary neutrophils fromperipheralblood	blood
28	chr3:100348400-100349200	Enhancers	Duodenum Mucosa	Duodenum
29	chr3:100348400-100349400	Enhancers	Fetal Intestine Small	intestine
30	chr3:100348400-100350600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr3:100348400-100350600	Enhancers	HMEC	breast
32	chr3:100348600-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr3:100348600-100350200	Enhancers	Hela-S3	cervix
34	chr3:100348600-100350400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr3:100348600-100353400	Weak transcription	Primary hematopoietic stem cells	blood
36	chr3:100348600-100354200	Weak transcription	Sigmoid Colon	Sigmoid Colon
37	chr3:100348800-100349800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr3:100349000-100350400	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr3:100349000-100350600	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr3:100349000-100350600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
41	chr3:100349200-100349400	Enhancers	Small Intestine	intestine
42	chr3:100349200-100350200	Enhancers	A549	lung
43	chr3:100349200-100350400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr3:100349200-100350400	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr3:100349200-100350600	Enhancers	iPS-20b Cell Line	embryonic stem cell
46	chr3:100349200-100352400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr3:100349400-100352800	Weak transcription	Fetal Intestine Small	intestine
48	chr3:100349600-100349800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:100349600-100349800	Bivalent Enhancer	NHDF-Ad	bronchial
50	chr3:100349600-100350400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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