Variant report

Variant	esv3374702
Chromosome Location	chr3:135649303-135686527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:312)
CpG islands
(count:795)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:312 , 50 per page) page: 1 2 3 4 5 6 7

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	CBX3	chr3:135676125-135676375	K562	blood:	n/a	n/a
3	CBX3	chr3:135676094-135676435	K562	blood:	n/a	n/a
4	CCNT2	chr3:135684228-135685385	K562	blood:	n/a	chr3:135685152-135685161
5	CEBPB	chr3:135678105-135678305	HepG2	liver:	n/a	n/a
6	CEBPB	chr3:135684827-135685231	Hela-S3	cervix:	n/a	n/a
7	CHD1	chr3:135685439-135685783	H1-hESC	embryonic stem cell:	n/a	n/a
8	CHD2	chr3:135685095-135685475	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr3:135685247-135685376	HepG2	liver:	n/a	n/a
10	CHD2	chr3:135684539-135684657	K562	blood:	n/a	n/a
11	CHD2	chr3:135684198-135684785	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr3:135683325-135683638	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr3:135685033-135685259	Hela-S3	cervix:	n/a	n/a
14	CREB1	chr3:135684447-135685078	HepG2	liver:	n/a	n/a
15	CREB1	chr3:135684136-135684707	A549	lung:	n/a	n/a
16	CTCF	chr3:135685320-135685360	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr3:135655532-135655589	GM20000	blood:	n/a	n/a
18	CTCF	chr3:135684160-135684310	HPAF	blood vessel:	n/a	n/a
19	CTCF	chr3:135684280-135684430	Caco-2	colon:	n/a	chr3:135684385-135684394
20	CTCF	chr3:135685180-135685330	HAc	cerebellar:	n/a	chr3:135685234-135685247 chr3:135685280-135685290 chr3:135685279-135685292
21	CTCF	chr3:135684140-135684410	BJ	skin:	n/a	chr3:135684385-135684394
22	CTCF	chr3:135685320-135685470	HCPEpiC	choroid plexus:	n/a	n/a
23	CTCF	chr3:135684020-135684170	SK-N-SH_RA	brain:	n/a	n/a
24	CTCF	chr3:135685288-135685420	MCF-7	breast:	n/a	n/a
25	CTCF	chr3:135685340-135685490	AG10803	skin:	n/a	n/a
26	CTCF	chr3:135684940-135685090	AG04449	skin:	n/a	n/a
27	CTCF	chr3:135685280-135685430	AG04449	skin:	n/a	chr3:135685280-135685290
28	CTCF	chr3:135685300-135685450	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr3:135685286-135685419	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:135684240-135684390	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr3:135676300-135676383	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr3:135684313-135684356	MCF-7	breast:	n/a	n/a
33	CTCF	chr3:135685220-135685370	SK-N-SH_RA	brain:	n/a	chr3:135685234-135685247 chr3:135685280-135685290 chr3:135685279-135685292
34	CTCF	chr3:135650286-135650327	Fibrobl	skin:	n/a	n/a
35	CTCF	chr3:135684297-135684405	MCF-7	breast:	n/a	chr3:135684385-135684394
36	CTCF	chr3:135685260-135685410	AG04449	skin:	n/a	chr3:135685280-135685290 chr3:135685279-135685292
37	CTCF	chr3:135684080-135684230	HRE	kidney:	n/a	n/a
38	CTCF	chr3:135685302-135685428	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:135684260-135684410	HCPEpiC	choroid plexus:	n/a	chr3:135684385-135684394
40	CTCF	chr3:135684260-135684410	HMEC	breast:	n/a	chr3:135684385-135684394
41	CTCF	chr3:135685100-135685250	NHLF	lung:	n/a	chr3:135685234-135685247
42	CTCF	chr3:135685320-135685470	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr3:135685240-135685390	HCM	heart:	n/a	chr3:135685280-135685290 chr3:135685279-135685292
44	CTCF	chr3:135675760-135675910	BE2_C	brain:	n/a	n/a
45	CTCF	chr3:135684240-135684390	AG04450	lung:	n/a	n/a
46	CTCF	chr3:135685300-135685450	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr3:135684260-135684410	HBMEC	blood vessel:	n/a	chr3:135684385-135684394
48	CTCF	chr3:135684890-135684943	Fibrobl	skin:	n/a	n/a
49	CTCF	chr3:135685340-135685490	NHLF	lung:	n/a	n/a
50	CTCF	chr3:135685240-135685390	AG09319	gingival:	n/a	chr3:135685280-135685290 chr3:135685279-135685292

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:135684107-135684157	Caco-2	colon:	n/a
2	chr3:135684161-135684211	A549	lung:	n/a
3	chr3:135684107-135684157	Caco-2	colon:	n/a
4	chr3:135684161-135684211	A549	lung:	n/a
5	chr3:135684466-135684516	HRPEpiC	eye:	n/a
6	chr3:135684468-135684518	HCF	heart:	n/a
7	chr3:135684161-135684211	HMEC	breast:	n/a
8	chr3:135684688-135684738	ovcar-3	ovarian:	n/a
9	chr3:135684439-135684489	IMR90	lung:	fetal
10	chr3:135684468-135684518	NT2-D1	testis:	n/a
11	chr3:135684466-135684516	Hepatocyte	liver:	n/a
12	chr3:135684439-135684489	SAEC	small airway:	n/a
13	chr3:135685428-135685478	ECC-1	luminal epithelium:	n/a
14	chr3:135685428-135685478	K562	blood:	n/a
15	chr3:135684107-135684157	HUVEC	blood vessel:	n/a
16	chr3:135684163-135684213	RPTEC	kidney:	n/a
17	chr3:135685428-135685478	A549	lung:	n/a
18	chr3:135685131-135685181	PrEC	prostate:	n/a
19	chr3:135684445-135684495	HMEC	breast:	n/a
20	chr3:135684107-135684157	IMR90	lung:	fetal
21	chr3:135684466-135684516	GM12892	blood:	n/a
22	chr3:135684439-135684489	MCF-7	breast:	n/a
23	chr3:135685098-135685148	MCF10A-Er-Src	breast:	n/a
24	chr3:135685098-135685148	NHBE	bronchial:	n/a
25	chr3:135684439-135684489	H1-hESC	embryonic stem cell:	embryo
26	chr3:135684688-135684738	HRPEpiC	eye:	n/a
27	chr3:135685131-135685181	NHDF-neo	bronchial:	n/a
28	chr3:135685098-135685148	HNPCEpiC	eye:	n/a
29	chr3:135685131-135685181	HCT-116	colon:	n/a
30	chr3:135684107-135684157	Jurkat	blood:	n/a
31	chr3:135685428-135685478	AG04449	skin:	fetal
32	chr3:135684439-135684489	GM12892	blood:	n/a
33	chr3:135685042-135685092	SAEC	small airway:	n/a
34	chr3:135685131-135685181	HAEpiC	amniotic membrane:	n/a
35	chr3:135685428-135685478	GM12878	blood:	n/a
36	chr3:135684161-135684211	PANC-1	pancreas:	n/a
37	chr3:135684468-135684518	GM12892	blood:	n/a
38	chr3:135684688-135684738	HNPCEpiC	eye:	n/a
39	chr3:135684688-135684738	AoSMC	blood vessel:	n/a
40	chr3:135684466-135684516	NHDF-neo	bronchial:	n/a
41	chr3:135685428-135685478	HCT-116	colon:	n/a
42	chr3:135684688-135684738	GM12891	blood:	n/a
43	chr3:135685428-135685478	MCF10A-Er-Src	breast:	n/a
44	chr3:135685098-135685148	T-47D	breast:	n/a
45	chr3:135684439-135684489	HNPCEpiC	eye:	n/a
46	chr3:135684468-135684518	A549	lung:	n/a
47	chr3:135684468-135684518	RPTEC	kidney:	n/a
48	chr3:135684163-135684213	H1-hESC	embryonic stem cell:	embryo
49	chr3:135685098-135685148	HRCEpiC	kidney:	n/a
50	chr3:135684161-135684211	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr3:135675046..135677818-chr3:135681944..135685047,4	MCF-7	breast:
2	chr3:135679723..135681371-chr3:135684487..135687101,2	MCF-7	breast:
3	chr3:135649256..135651506-chr3:135683759..135686292,2	MCF-7	breast:
4	chr3:135626053..135627736-chr3:135684595..135686166,2	MCF-7	breast:
5	chr3:135678002..135681918-chr3:135682555..135686339,5	MCF-7	breast:
6	chr3:135678002..135681918-chr3:135682555..135686339,5	MCF-7	breast:
7	chr3:135683335..135686243-chr3:135740274..135744209,4	MCF-7	breast:
8	chr3:134446614..134448331-chr3:135662796..135664940,2	K562	blood:
9	chr3:135674887..135676860-chr3:135678363..135680009,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000241905	TF binding region
PPP2R3A	TF binding region
ENSG00000256425	TF binding region
ENSG00000241905	CpG island
PPP2R3A	CpG island
ENSG00000256425	CpG island
ENSG00000241905	chromatin interactions
ENSG00000073711	chromatin interactions

Extended variants
information (count: 770 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:770 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10512981	chr3:135649310-135649311	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs539345293	chr3:135649334-135649335	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563944851	chr3:135649355-135649356	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs558654038	chr3:135649359-135649360	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs532838502	chr3:135649360-135649361	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140357986	chr3:135649388-135649389	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs555247622	chr3:135649421-135649422	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs116597875	chr3:135649501-135649502	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs528912133	chr3:135649512-135649513	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs549408925	chr3:135649535-135649536	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184922028	chr3:135649543-135649544	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs189767112	chr3:135649646-135649647	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs572489966	chr3:135649676-135649677	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537464811	chr3:135649710-135649711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs551957898	chr3:135649713-135649714	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557406202	chr3:135649749-135649750	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs115797106	chr3:135649756-135649757	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs76628139	chr3:135649794-135649795	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs539985985	chr3:135649831-135649832	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs567529619	chr3:135649848-135649849	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs371320275	chr3:135649865-135649866	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs536695363	chr3:135649887-135649888	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs368610838	chr3:135649940-135649941	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs372221296	chr3:135649986-135649987	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs541497904	chr3:135649991-135649992	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs559885643	chr3:135650006-135650007	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs145563573	chr3:135650020-135650021	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs557498203	chr3:135650047-135650048	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs577451435	chr3:135650048-135650049	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs7640153	chr3:135650060-135650061	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs138165409	chr3:135650095-135650096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs560241103	chr3:135650124-135650125	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111777741	chr3:135650151-135650152	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs36055666	chr3:135650210-135650211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs542493577	chr3:135650257-135650258	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528873357	chr3:135650258-135650259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs140995763	chr3:135650259-135650260	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs61569459	chr3:135650269-135650270	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs192515539	chr3:135650281-135650282	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs183596184	chr3:135650307-135650308	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs189364004	chr3:135650313-135650314	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181732029	chr3:135650326-135650327	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571853280	chr3:135650391-135650392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs373562034	chr3:135650393-135650394	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs527912194	chr3:135650407-135650408	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs114241109	chr3:135650408-135650409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs368044603	chr3:135650417-135650418	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542816311	chr3:135650456-135650457	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs59343603	chr3:135650462-135650463	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs536353442	chr3:135650479-135650480	Weak transcription	Chromatin interactive region	1 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:511 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:135647800-135649400	Enhancers	Fetal Muscle Leg	muscle
2	chr3:135648000-135649400	Enhancers	Breast Myoepithelial Primary Cells	Breast
3	chr3:135648000-135649400	Enhancers	Duodenum Smooth Muscle	Duodenum
4	chr3:135648000-135649400	Enhancers	Skeletal Muscle Female	skeletal muscle
5	chr3:135648000-135649400	Enhancers	NHDF-Ad	bronchial
6	chr3:135648000-135649600	Enhancers	Colon Smooth Muscle	Colon
7	chr3:135648000-135649600	Enhancers	Rectal Smooth Muscle	rectum
8	chr3:135648000-135649600	Enhancers	HSMMtube	muscle
9	chr3:135648400-135649400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr3:135648400-135649400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr3:135648400-135649400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr3:135648400-135649600	Enhancers	Placenta Amnion	Placenta Amnion
13	chr3:135648400-135649600	Enhancers	HSMM	muscle
14	chr3:135648600-135649400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr3:135648600-135649400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr3:135648600-135649400	Enhancers	Brain Substantia Nigra	brain
17	chr3:135648600-135649400	Enhancers	Fetal Stomach	stomach
18	chr3:135648600-135649400	Enhancers	Right Ventricle	heart
19	chr3:135648600-135649400	Enhancers	HMEC	breast
20	chr3:135648800-135649400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr3:135649000-135649400	Flanking Active TSS	Fetal Heart	heart
22	chr3:135649000-135653200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr3:135649200-135649400	Enhancers	Psoas Muscle	Psoas
24	chr3:135649200-135649400	Flanking Active TSS	Stomach Smooth Muscle	stomach
25	chr3:135649200-135653800	Weak transcription	NHEK	skin
26	chr3:135649400-135650000	Enhancers	Fetal Heart	heart
27	chr3:135649600-135653600	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr3:135653200-135654200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr3:135653400-135655800	Enhancers	Placenta	Placenta
30	chr3:135653600-135654000	Enhancers	Placenta Amnion	Placenta Amnion
31	chr3:135653800-135654400	Enhancers	NHEK	skin
32	chr3:135663200-135663600	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr3:135663200-135664000	Enhancers	Skeletal Muscle Male	skeletal muscle
34	chr3:135663200-135664600	Enhancers	Fetal Muscle Leg	muscle
35	chr3:135663200-135664600	Enhancers	HSMM	muscle
36	chr3:135663200-135664600	Enhancers	HSMMtube	muscle
37	chr3:135663400-135664600	Enhancers	Psoas Muscle	Psoas
38	chr3:135663600-135663800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr3:135663600-135664200	Enhancers	Muscle Satellite Cultured Cells	--
40	chr3:135663600-135664200	Enhancers	Fetal Muscle Trunk	muscle
41	chr3:135663600-135664400	Enhancers	Placenta	Placenta
42	chr3:135663600-135664400	Enhancers	Osteobl	bone
43	chr3:135663800-135664000	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr3:135664000-135664200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
45	chr3:135664000-135664400	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr3:135664000-135664400	Enhancers	NHDF-Ad	bronchial
47	chr3:135664000-135664400	Enhancers	NHLF	lung
48	chr3:135664200-135664800	Enhancers	Skeletal Muscle Female	skeletal muscle
49	chr3:135664400-135664600	Enhancers	Skeletal Muscle Male	skeletal muscle
50	chr3:135668600-135669800	Enhancers	Fetal Brain Male	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links