Variant report

Variant	nsv877144
Chromosome Location	chr3:87691029-87845957
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:923)
CpG islands
(count:549)
Chromatin interactive
region (count:29)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:923 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:87820565-87820676	K562	blood:	n/a	n/a
2	ARID3A	chr3:87837578-87837623	K562	blood:	n/a	n/a
3	ARID3A	chr3:87845165-87845971	K562	blood:	n/a	n/a
4	ATF1	chr3:87845222-87845685	K562	blood:	n/a	n/a
5	ATF1	chr3:87839831-87840243	K562	blood:	n/a	n/a
6	ATF2	chr3:87723828-87724353	GM12878	blood:	n/a	n/a
7	ATF2	chr3:87723887-87724325	GM12878	blood:	n/a	n/a
8	ATF3	chr3:87845316-87845788	K562	blood:	n/a	n/a
9	BACH1	chr3:87841407-87841692	K562	blood:	n/a	n/a
10	BACH1	chr3:87841454-87842181	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:87820557-87820578	K562	blood:	n/a	n/a
12	BCL11A	chr3:87777026-87777188	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr3:87723898-87724281	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:87776930-87777274	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr3:87723571-87723850	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:87723845-87724273	GM12878	blood:	n/a	n/a
17	BCLAF1	chr3:87845143-87845687	K562	blood:	n/a	n/a
18	BHLHE40	chr3:87841624-87842476	K562	blood:	n/a	chr3:87841931-87841947 chr3:87841808-87841824 chr3:87841972-87841988 chr3:87842037-87842053
19	BHLHE40	chr3:87842682-87842708	K562	blood:	n/a	n/a
20	BHLHE40	chr3:87820480-87820751	GM12878	blood:	n/a	n/a
21	BHLHE40	chr3:87845112-87845719	K562	blood:	n/a	n/a
22	BHLHE40	chr3:87723553-87724426	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:87844618-87844835	K562	blood:	n/a	n/a
24	CBX3	chr3:87789999-87790224	K562	blood:	n/a	n/a
25	CBX3	chr3:87790020-87790221	K562	blood:	n/a	n/a
26	CBX3	chr3:87845223-87845642	K562	blood:	n/a	n/a
27	CBX3	chr3:87805024-87805380	K562	blood:	n/a	n/a
28	CCNT2	chr3:87841691-87842470	K562	blood:	n/a	chr3:87841941-87841950
29	CCNT2	chr3:87845078-87845730	K562	blood:	n/a	n/a
30	CEBPB	chr3:87836998-87837238	A549	lung:	n/a	chr3:87837140-87837149 chr3:87837139-87837150 chr3:87837138-87837149
31	CEBPB	chr3:87820427-87820732	IMR90	lung:	n/a	n/a
32	CEBPB	chr3:87820432-87820745	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr3:87843797-87844383	K562	blood:	n/a	n/a
34	CEBPB	chr3:87745305-87745603	K562	blood:	n/a	n/a
35	CEBPB	chr3:87820405-87820749	K562	blood:	n/a	n/a
36	CEBPB	chr3:87751750-87752093	HepG2	liver:	n/a	n/a
37	CEBPB	chr3:87733900-87734091	K562	blood:	n/a	n/a
38	CEBPB	chr3:87844169-87844247	A549	lung:	n/a	n/a
39	CEBPB	chr3:87839951-87840158	A549	lung:	n/a	n/a
40	CEBPB	chr3:87820473-87820641	HepG2	liver:	n/a	n/a
41	CEBPB	chr3:87751861-87751982	A549	lung:	n/a	n/a
42	CEBPB	chr3:87820451-87820773	HepG2	liver:	n/a	n/a
43	CEBPB	chr3:87751904-87751914	K562	blood:	n/a	n/a
44	CEBPB	chr3:87837002-87837299	HepG2	liver:	n/a	chr3:87837140-87837149 chr3:87837139-87837150 chr3:87837138-87837149
45	CEBPB	chr3:87724224-87724507	HepG2	liver:	n/a	chr3:87724379-87724390 chr3:87724380-87724391 chr3:87724379-87724392
46	CEBPB	chr3:87844091-87844252	K562	blood:	n/a	n/a
47	CEBPB	chr3:87820369-87820797	MCF-7	breast:	n/a	n/a
48	CEBPB	chr3:87839887-87840188	K562	blood:	n/a	n/a
49	CEBPB	chr3:87777041-87777308	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr3:87830067-87830293	K562	blood:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:87729320-87729370	Jurkat	blood:	n/a
2	chr3:87843755-87843805	PrEC	prostate:	n/a
3	chr3:87842398-87842448	PrEC	prostate:	n/a
4	chr3:87842246-87842296	ovcar-3	ovarian:	n/a
5	chr3:87839841-87839891	HNPCEpiC	eye:	n/a
6	chr3:87811194-87811244	SK-N-MC	brain:	n/a
7	chr3:87843755-87843805	GM12892	blood:	n/a
8	chr3:87729320-87729370	MCF-7	breast:	n/a
9	chr3:87842246-87842296	AG09319	gingival:	n/a
10	chr3:87810762-87810812	NH-A	brain:	n/a
11	chr3:87810762-87810812	CMK	blood:	n/a
12	chr3:87842398-87842448	HPAEpiC	pulmonary alveolar:	n/a
13	chr3:87811194-87811244	SK-N-SH_RA	brain:	n/a
14	chr3:87842019-87842069	RPTEC	kidney:	n/a
15	chr3:87843755-87843805	HUVEC	blood vessel:	n/a
16	chr3:87810762-87810812	AG09319	gingival:	n/a
17	chr3:87810762-87810812	HRPEpiC	eye:	n/a
18	chr3:87842019-87842069	H1-hESC	embryonic stem cell:	embryo
19	chr3:87842398-87842448	ovcar-3	ovarian:	n/a
20	chr3:87729320-87729370	MCF10A-Er-Src	breast:	n/a
21	chr3:87728433-87728483	HNPCEpiC	eye:	n/a
22	chr3:87728433-87728483	HCT-116	colon:	n/a
23	chr3:87810762-87810812	HUVEC	blood vessel:	n/a
24	chr3:87811194-87811244	SK-N-SH	brain:	n/a
25	chr3:87810762-87810812	NT2-D1	testis:	n/a
26	chr3:87843755-87843805	NHDF-neo	bronchial:	n/a
27	chr3:87842246-87842296	HMEC	breast:	n/a
28	chr3:87811194-87811244	PANC-1	pancreas:	n/a
29	chr3:87728433-87728483	GM12892	blood:	n/a
30	chr3:87811194-87811244	ProgFib	skin:	n/a
31	chr3:87843755-87843805	BE2_C	brain:	n/a
32	chr3:87842019-87842069	AG04450	lung:	fetal
33	chr3:87839841-87839891	AG10803	skin:	n/a
34	chr3:87842246-87842296	SK-N-SH_RA	brain:	n/a
35	chr3:87729320-87729370	AG10803	skin:	n/a
36	chr3:87842398-87842448	RPTEC	kidney:	n/a
37	chr3:87839841-87839891	PFSK-1	brain:	n/a
38	chr3:87842019-87842069	SK-N-SH	brain:	n/a
39	chr3:87842019-87842069	ProgFib	skin:	n/a
40	chr3:87842019-87842069	GM12878	blood:	n/a
41	chr3:87810762-87810812	HNPCEpiC	eye:	n/a
42	chr3:87843755-87843805	Hepatocyte	liver:	n/a
43	chr3:87728433-87728483	HepG2	liver:	n/a
44	chr3:87729320-87729370	T-47D	breast:	n/a
45	chr3:87842398-87842448	K562	blood:	n/a
46	chr3:87842246-87842296	K562	blood:	n/a
47	chr3:87811194-87811244	AG04449	skin:	fetal
48	chr3:87842246-87842296	PrEC	prostate:	n/a
49	chr3:87729320-87729370	AG09319	gingival:	n/a
50	chr3:87839841-87839891	HCF	heart:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:87845525..87848228-chr3:87871993..87873515,2	K562	blood:
2	chr3:87346989..87347924-chr3:87820302..87821498,3	MCF-7	breast:
3	chr3:87774485..87776498-chr3:87777273..87779870,3	MCF-7	breast:
4	chr3:87835402..87838110-chr3:87839403..87841793,3	K562	blood:
5	chr3:87773985..87776726-chr3:87783571..87785837,2	MCF-7	breast:
6	chr3:87835402..87838110-chr3:87839403..87841793,3	K562	blood:
7	chr3:87805200..87807448-chr3:87809033..87811045,2	K562	blood:
8	chr3:87787506..87789179-chr3:87800683..87802189,2	MCF-7	breast:
9	chr3:87789321..87792117-chr3:87796229..87798081,2	MCF-7	breast:
10	chr3:87773985..87776726-chr3:87783571..87785837,2	MCF-7	breast:
11	chr3:87715509..87718110-chr3:87725077..87727832,2	MCF-7	breast:
12	chr3:87805630..87807898-chr3:87809132..87811197,2	MCF-7	breast:
13	chr3:87808352..87810255-chr3:87812136..87814576,2	MCF-7	breast:
14	chr3:87715509..87718110-chr3:87725077..87727832,2	MCF-7	breast:
15	chr3:87787506..87789179-chr3:87800683..87802189,2	MCF-7	breast:
16	chr3:87827898..87830613-chr3:87841535..87843509,2	K562	blood:
17	chr3:87820271..87821383-chr3:88051902..88052924,6	MCF-7	breast:
18	chr3:87347562..87348198-chr3:87820743..87821251,2	MCF-7	breast:
19	chr3:87745181..87747327-chr3:87772407..87775801,3	K562	blood:
20	chr3:87843885..87846211-chr3:87904754..87906414,2	K562	blood:
21	chr3:87808352..87810255-chr3:87812136..87814576,2	MCF-7	breast:
22	chr3:87805630..87807898-chr3:87809132..87811197,2	MCF-7	breast:
23	chr3:87752670..87754550-chr3:87776800..87779392,2	MCF-7	breast:
24	chr3:87805200..87807448-chr3:87809033..87811045,2	K562	blood:
25	chr3:87745181..87747327-chr3:87772407..87775801,3	K562	blood:
26	chr3:87752670..87754550-chr3:87776800..87779392,2	MCF-7	breast:
27	chr3:87820697..87821585-chr3:88052369..88052934,2	MCF-7	breast:
28	chr3:87834701..87839368-chr3:87839393..87843561,7	K562	blood:
29	chr3:87774485..87776498-chr3:87777273..87779870,3	MCF-7	breast:

No data

Variant related genes	Relation type
RNU6-873P	TF binding region
ENSG00000239572	TF binding region
RNU6-873P	CpG island
ENSG00000239572	CpG island
ENSG00000239572	chromatin interactions
ENSG00000200703	chromatin interactions

Extended variants
information (count: 2750 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:2750 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4569679	chr3:87691029-87691030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550142627	chr3:87691048-87691049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74884721	chr3:87691054-87691055	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs79903854	chr3:87691055-87691056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs77231142	chr3:87691068-87691069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116035327	chr3:87691091-87691092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs554651296	chr3:87691146-87691147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573158483	chr3:87691164-87691165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs534056256	chr3:87691232-87691233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558580876	chr3:87691300-87691301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148136742	chr3:87691305-87691306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs542743975	chr3:87691308-87691309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs544396941	chr3:87691369-87691370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs534613556	chr3:87691384-87691385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs371328863	chr3:87691390-87691391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141698911	chr3:87691476-87691477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190075502	chr3:87691480-87691481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs9838106	chr3:87691551-87691552	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs557963058	chr3:87691585-87691586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576250231	chr3:87691606-87691607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145968226	chr3:87691613-87691614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs139832864	chr3:87691642-87691643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527236305	chr3:87691710-87691711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs74339340	chr3:87691712-87691713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs182708567	chr3:87691713-87691714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186474043	chr3:87691729-87691730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs192737646	chr3:87691743-87691744	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs111441319	chr3:87691768-87691769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs544278715	chr3:87691786-87691787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs183705288	chr3:87691799-87691800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368637980	chr3:87691823-87691824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189146708	chr3:87691836-87691837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs528035877	chr3:87691837-87691838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547641734	chr3:87691839-87691840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566755334	chr3:87691849-87691850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368195105	chr3:87691868-87691869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533922087	chr3:87691934-87691935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs9839050	chr3:87691945-87691946	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs576903239	chr3:87691958-87691959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs376292393	chr3:87691984-87691985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs13092678	chr3:87692006-87692007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs141538624	chr3:87692040-87692041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193127511	chr3:87692096-87692097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs574946119	chr3:87692101-87692102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542159662	chr3:87692189-87692190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554403125	chr3:87692243-87692244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184472272	chr3:87692244-87692245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs189226117	chr3:87692259-87692260	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs146168376	chr3:87692263-87692264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs531421146	chr3:87692290-87692291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Acute myeloid leukemia	20729466	CNVD
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
Acute lymphoblastic leukemia	20435627	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
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Wilms tumour	21544195	CNVD
Soft tissue tumor	16732325	CNVD
small cell lung cancer	20016488	CNVD
Neurodevelopmental disorder	22521361	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
craniofacial dysmorphism	21918468	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	21829676	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:479 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:87687600-87694000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:87693800-87694200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
3	chr3:87693800-87694200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr3:87694000-87695400	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr3:87694000-87695600	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr3:87694000-87695600	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr3:87694000-87695600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr3:87694200-87695200	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr3:87694200-87695200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr3:87695200-87695400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr3:87695200-87695400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:87702600-87702800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:87702800-87703000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr3:87702800-87703600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr3:87703600-87706000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:87722800-87723200	Bivalent Enhancer	GM12878-XiMat	blood
17	chr3:87723200-87724600	Enhancers	GM12878-XiMat	blood
18	chr3:87723600-87724400	Enhancers	Primary B cells from peripheral blood	blood
19	chr3:87723600-87724600	Bivalent Enhancer	Primary B cells from cord blood	blood
20	chr3:87724000-87724400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr3:87724000-87724400	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
22	chr3:87724200-87724400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
23	chr3:87724200-87724400	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood
24	chr3:87728800-87732000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr3:87739600-87740000	Enhancers	HMEC	breast
26	chr3:87740000-87740400	Enhancers	NHEK	skin
27	chr3:87743800-87744000	Enhancers	HSMMtube	muscle
28	chr3:87744200-87744600	Enhancers	Fetal Muscle Leg	muscle
29	chr3:87744200-87745400	Weak transcription	HSMMtube	muscle
30	chr3:87744600-87745000	Weak transcription	Fetal Muscle Leg	muscle
31	chr3:87745000-87745800	Enhancers	Fetal Muscle Leg	muscle
32	chr3:87745400-87746000	Enhancers	HSMMtube	muscle
33	chr3:87745600-87746000	Enhancers	K562	blood
34	chr3:87754600-87754800	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr3:87754600-87756600	Enhancers	Primary monocytes fromperipheralblood	blood
36	chr3:87754800-87755200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
37	chr3:87755000-87755600	Enhancers	HMEC	breast
38	chr3:87755200-87755600	Enhancers	Primary neutrophils fromperipheralblood	blood
39	chr3:87755200-87756400	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr3:87756200-87756800	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr3:87756400-87759200	Weak transcription	Monocytes-CD14+_RO01746	blood
42	chr3:87756800-87765600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr3:87759200-87760000	Enhancers	Monocytes-CD14+_RO01746	blood
44	chr3:87759600-87760000	Active TSS	Fetal Heart	heart
45	chr3:87765600-87766000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr3:87775000-87775200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr3:87775000-87775800	Enhancers	HUVEC	blood vessel
48	chr3:87775200-87776600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:87775200-87779000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
50	chr3:87775400-87775800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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