Variant report

Variant	esv3393718
Chromosome Location	chr3:135683487-135686235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:270)
CpG islands
(count:732)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:270 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr3:135684536-135684676	K562	blood:	n/a	n/a
2	CCNT2	chr3:135684228-135685385	K562	blood:	n/a	chr3:135685152-135685161
3	CEBPB	chr3:135684827-135685231	Hela-S3	cervix:	n/a	n/a
4	CHD1	chr3:135685439-135685783	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr3:135685247-135685376	HepG2	liver:	n/a	n/a
6	CHD2	chr3:135684198-135684785	H1-hESC	embryonic stem cell:	n/a	n/a
7	CHD2	chr3:135685095-135685475	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr3:135683325-135683638	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr3:135685033-135685259	Hela-S3	cervix:	n/a	n/a
10	CHD2	chr3:135684539-135684657	K562	blood:	n/a	n/a
11	CREB1	chr3:135684447-135685078	HepG2	liver:	n/a	n/a
12	CREB1	chr3:135684136-135684707	A549	lung:	n/a	n/a
13	CTCF	chr3:135684240-135684390	AG04450	lung:	n/a	n/a
14	CTCF	chr3:135684240-135684390	SK-N-SH_RA	brain:	n/a	n/a
15	CTCF	chr3:135685280-135685430	AG04449	skin:	n/a	chr3:135685280-135685290
16	CTCF	chr3:135685349-135685388	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:135684260-135684410	HCPEpiC	choroid plexus:	n/a	chr3:135684385-135684394
18	CTCF	chr3:135684260-135684410	HBMEC	blood vessel:	n/a	chr3:135684385-135684394
19	CTCF	chr3:135685300-135685450	SK-N-SH_RA	brain:	n/a	n/a
20	CTCF	chr3:135684020-135684170	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr3:135684240-135684390	AG10803	skin:	n/a	n/a
22	CTCF	chr3:135685340-135685490	AG10803	skin:	n/a	n/a
23	CTCF	chr3:135684280-135684430	Caco-2	colon:	n/a	chr3:135684385-135684394
24	CTCF	chr3:135685320-135685470	HCPEpiC	choroid plexus:	n/a	n/a
25	CTCF	chr3:135684200-135684350	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr3:135684280-135684430	AG04449	skin:	n/a	chr3:135684385-135684394
27	CTCF	chr3:135684180-135684330	HCFaa	heart:	n/a	n/a
28	CTCF	chr3:135684940-135685090	AG04449	skin:	n/a	n/a
29	CTCF	chr3:135684140-135684410	BJ	skin:	n/a	chr3:135684385-135684394
30	CTCF	chr3:135685240-135685390	AG09319	gingival:	n/a	chr3:135685280-135685290 chr3:135685279-135685292
31	CTCF	chr3:135685240-135685390	HCM	heart:	n/a	chr3:135685280-135685290 chr3:135685279-135685292
32	CTCF	chr3:135684313-135684356	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:135684260-135684410	HMEC	breast:	n/a	chr3:135684385-135684394
34	CTCF	chr3:135685340-135685490	NHLF	lung:	n/a	n/a
35	CTCF	chr3:135685200-135685350	GM12874	blood:	n/a	chr3:135685234-135685247 chr3:135685280-135685290 chr3:135685279-135685292
36	CTCF	chr3:135685320-135685470	AoAF	blood vessel:	n/a	n/a
37	CTCF	chr3:135685277-135685384	SK-N-SH_RA	brain:	n/a	chr3:135685280-135685290 chr3:135685279-135685292
38	CTCF	chr3:135684890-135684943	Fibrobl	skin:	n/a	n/a
39	CTCF	chr3:135685302-135685428	MCF-7	breast:	n/a	n/a
40	CTCF	chr3:135684080-135684230	HRE	kidney:	n/a	n/a
41	CTCF	chr3:135685320-135685360	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr3:135684297-135684405	MCF-7	breast:	n/a	chr3:135684385-135684394
43	CTCF	chr3:135685220-135685370	SK-N-SH_RA	brain:	n/a	chr3:135685234-135685247 chr3:135685280-135685290 chr3:135685279-135685292
44	CTCF	chr3:135684240-135684390	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr3:135684160-135684310	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr3:135685100-135685250	NHLF	lung:	n/a	chr3:135685234-135685247
47	CTCF	chr3:135685280-135685430	AG09309	skin:	n/a	chr3:135685280-135685290
48	CTCF	chr3:135685300-135685450	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr3:135684304-135684406	MCF-7	breast:	n/a	chr3:135684385-135684394
50	CTCF	chr3:135685280-135685430	AG09319	gingival:	n/a	chr3:135685280-135685290

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:135685131-135685181	HAEpiC	amniotic membrane:	n/a
2	chr3:135684163-135684213	SK-N-SH	brain:	n/a
3	chr3:135685098-135685148	ECC-1	luminal epithelium:	n/a
4	chr3:135684439-135684489	MCF-7	breast:	n/a
5	chr3:135684161-135684211	PrEC	prostate:	n/a
6	chr3:135684466-135684516	NHBE	bronchial:	n/a
7	chr3:135684107-135684157	HepG2	liver:	n/a
8	chr3:135684107-135684157	CMK	blood:	n/a
9	chr3:135684445-135684495	NB4	blood:	n/a
10	chr3:135685098-135685148	HRE	kidney:	n/a
11	chr3:135684161-135684211	HEEpiC	esophagus:	n/a
12	chr3:135685428-135685478	T-47D	breast:	n/a
13	chr3:135685428-135685478	AG10803	skin:	n/a
14	chr3:135685428-135685478	MCF-7	breast:	n/a
15	chr3:135684163-135684213	Hela-S3	cervix:	n/a
16	chr3:135684439-135684489	HIPEpiC	eye:	n/a
17	chr3:135684445-135684495	Hepatocyte	liver:	n/a
18	chr3:135684439-135684489	AG10803	skin:	n/a
19	chr3:135684439-135684489	AG09319	gingival:	n/a
20	chr3:135685098-135685148	BE2_C	brain:	n/a
21	chr3:135684163-135684213	HRPEpiC	eye:	n/a
22	chr3:135684468-135684518	HCT-116	colon:	n/a
23	chr3:135684161-135684211	MCF-7	breast:	n/a
24	chr3:135684107-135684157	HCT-116	colon:	n/a
25	chr3:135685042-135685092	AG04450	lung:	fetal
26	chr3:135684163-135684213	ProgFib	skin:	n/a
27	chr3:135685428-135685478	GM12891	blood:	n/a
28	chr3:135685131-135685181	K562	blood:	n/a
29	chr3:135684161-135684211	BE2_C	brain:	n/a
30	chr3:135684163-135684213	CMK	blood:	n/a
31	chr3:135685042-135685092	SK-N-MC	brain:	n/a
32	chr3:135684439-135684489	NHBE	bronchial:	n/a
33	chr3:135684688-135684738	BJ	skin:	n/a
34	chr3:135685428-135685478	PrEC	prostate:	n/a
35	chr3:135684439-135684489	T-47D	breast:	n/a
36	chr3:135684688-135684738	HL-60	blood:	n/a
37	chr3:135684439-135684489	SAEC	small airway:	n/a
38	chr3:135684468-135684518	SK-N-SH_RA	brain:	n/a
39	chr3:135685131-135685181	Hela-S3	cervix:	n/a
40	chr3:135684163-135684213	MCF-7	breast:	n/a
41	chr3:135685131-135685181	PANC-1	pancreas:	n/a
42	chr3:135684468-135684518	GM12878	blood:	n/a
43	chr3:135684107-135684157	GM06990	blood:	n/a
44	chr3:135684466-135684516	ProgFib	skin:	n/a
45	chr3:135684439-135684489	H1-hESC	embryonic stem cell:	embryo
46	chr3:135684439-135684489	LNCaP	prostate:	n/a
47	chr3:135684688-135684738	SKMC	muscle:	n/a
48	chr3:135684163-135684213	GM12878	blood:	n/a
49	chr3:135684161-135684211	A549	lung:	n/a
50	chr3:135684107-135684157	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:135678002..135681918-chr3:135682555..135686339,5	MCF-7	breast:
2	chr3:135626053..135627736-chr3:135684595..135686166,2	MCF-7	breast:
3	chr3:135683335..135686243-chr3:135740274..135744209,4	MCF-7	breast:

No data

Variant related genes	Relation type
PPP2R3A	TF binding region
PPP2R3A	CpG island
ENSG00000241905	chromatin interactions
ENSG00000073711	chromatin interactions

Extended variants
information (count: 97 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:97 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115965283	chr3:135683504-135683505	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs576082345	chr3:135683528-135683529	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs9831808	chr3:135683531-135683532	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs368904310	chr3:135683558-135683559	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs544814550	chr3:135683589-135683590	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs372167461	chr3:135683611-135683612	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs576866115	chr3:135683636-135683637	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs75674033	chr3:135683668-135683669	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs527247195	chr3:135683691-135683692	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547013244	chr3:135683706-135683707	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs561215282	chr3:135683711-135683712	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs530363330	chr3:135683720-135683721	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs549941514	chr3:135683784-135683785	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs570201828	chr3:135683793-135683794	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs574973103	chr3:135683851-135683852	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs539114325	chr3:135683853-135683854	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs147514379	chr3:135683886-135683887	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs139935223	chr3:135683915-135683916	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs534981659	chr3:135683940-135683941	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs555036496	chr3:135683949-135683950	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs188133026	chr3:135683986-135683987	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs16843571	chr3:135684069-135684070	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs374816053	chr3:135684079-135684080	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs192825508	chr3:135684108-135684109	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs543924943	chr3:135684113-135684114	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs576114046	chr3:135684118-135684119	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs545189103	chr3:135684138-135684139	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs558343087	chr3:135684161-135684162	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs115698421	chr3:135684174-135684175	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs540611701	chr3:135684188-135684189	Active TSS Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs560581224	chr3:135684228-135684229	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs530325465	chr3:135684335-135684336	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs368921264	chr3:135684341-135684342	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs564020077	chr3:135684348-135684349	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs532552337	chr3:135684372-135684373	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs552751440	chr3:135684383-135684384	Active TSS Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs376889979	chr3:135684438-135684439	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs371301728	chr3:135684439-135684440	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs184442184	chr3:135684459-135684460	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs528623496	chr3:135684466-135684467	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs548599335	chr3:135684486-135684487	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs549524712	chr3:135684511-135684512	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs568505208	chr3:135684525-135684526	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs537449797	chr3:135684532-135684533	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs556135612	chr3:135684564-135684565	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs569957125	chr3:135684572-135684573	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs538423649	chr3:135684580-135684581	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs558753441	chr3:135684588-135684589	Active TSS Enhancers Bivalent/Poised TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs571788700	chr3:135684610-135684611	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs540774741	chr3:135684633-135684634	Active TSS Bivalent/Poised TSS Flanking Active TSS Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:54)

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
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135682400-135684000	Enhancers	H1 Cell Line	embryonic stem cell
2	chr3:135682600-135684000	Enhancers	Fetal Intestine Small	intestine
3	chr3:135682800-135684000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr3:135682800-135684200	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr3:135682800-135684600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr3:135683000-135683600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
7	chr3:135683000-135683800	Enhancers	Brain Inferior Temporal Lobe	brain
8	chr3:135683000-135683800	Enhancers	Rectal Mucosa Donor 29	rectum
9	chr3:135683000-135684000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:135683000-135684000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:135683000-135684000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr3:135683000-135684000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr3:135683000-135684000	Enhancers	Fetal Muscle Leg	muscle
14	chr3:135683000-135684200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
15	chr3:135683000-135684200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
16	chr3:135683000-135685800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
17	chr3:135683200-135683600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr3:135683200-135683800	Enhancers	Adipose Nuclei	Adipose
19	chr3:135683200-135683800	Enhancers	Brain Angular Gyrus	brain
20	chr3:135683200-135683800	Enhancers	Skeletal Muscle Female	skeletal muscle
21	chr3:135683200-135684000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
22	chr3:135683200-135684000	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr3:135683200-135684000	Enhancers	Liver	Liver
24	chr3:135683200-135684000	Enhancers	Brain Hippocampus Middle	brain
25	chr3:135683200-135684000	Enhancers	Duodenum Mucosa	Duodenum
26	chr3:135683200-135684000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr3:135683200-135684000	Enhancers	Fetal Heart	heart
28	chr3:135683200-135684000	Enhancers	Fetal Intestine Large	intestine
29	chr3:135683200-135684000	Enhancers	Right Ventricle	heart
30	chr3:135683200-135684200	Enhancers	Stomach Mucosa	stomach
31	chr3:135683400-135683600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr3:135683400-135683600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr3:135683400-135683600	Flanking Active TSS	Brain Substantia Nigra	brain
34	chr3:135683400-135683600	Enhancers	Small Intestine	intestine
35	chr3:135683400-135683800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr3:135683400-135683800	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr3:135683400-135683800	Enhancers	Brain Cingulate Gyrus	brain
38	chr3:135683400-135683800	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr3:135683400-135683800	Enhancers	Left Ventricle	heart
40	chr3:135683400-135683800	Enhancers	Ovary	ovary
41	chr3:135683400-135684000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr3:135683400-135684000	Enhancers	Pancreas	Pancrea
43	chr3:135683400-135684000	Enhancers	Rectal Smooth Muscle	rectum
44	chr3:135683400-135684000	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
45	chr3:135683400-135684200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
46	chr3:135683400-135684400	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr3:135683600-135683800	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr3:135683600-135683800	Active TSS	iPS-20b Cell Line	embryonic stem cell
49	chr3:135683600-135683800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
50	chr3:135683600-135683800	Enhancers	Brain Substantia Nigra	brain

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