Variant report

Variant	nsv961449
Chromosome Location	chr2:96069177-96081253
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:586)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:586 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr2:96079913-96080045	K562	blood:	n/a	n/a
2	BHLHE40	chr2:96068276-96069304	HepG2	liver:	n/a	chr2:96068367-96068383
3	BHLHE40	chr2:96079900-96080067	GM12878	blood:	n/a	n/a
4	BRCA1	chr2:96079869-96079881	HepG2	liver:	n/a	n/a
5	CEBPB	chr2:96077032-96077288	IMR90	lung:	n/a	n/a
6	CHD1	chr2:96079722-96080147	IMR90	lung:	n/a	n/a
7	CHD2	chr2:96079901-96080004	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTCF	chr2:96070588-96070739	GM13977	blood:	n/a	chr2:96070639-96070652
9	CTCF	chr2:96069220-96069370	HRE	kidney:	n/a	n/a
10	CTCF	chr2:96079820-96079970	HMEC	breast:	n/a	n/a
11	CTCF	chr2:96079780-96079930	NHEK	skin:	n/a	n/a
12	CTCF	chr2:96079837-96080093	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTCF	chr2:96079699-96080122	K562	blood:	n/a	n/a
14	CTCF	chr2:96079820-96079970	GM12865	blood:	n/a	n/a
15	CTCF	chr2:96079500-96079650	GM12870	blood:	n/a	n/a
16	CTCF	chr2:96069140-96069290	AG09309	skin:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
17	CTCF	chr2:96070620-96070770	Hela-S3	cervix:	n/a	chr2:96070639-96070652
18	CTCF	chr2:96079860-96080010	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr2:96079800-96080067	A549	lung:	n/a	n/a
20	CTCF	chr2:96079758-96080029	A549	lung:	n/a	n/a
21	CTCF	chr2:96069220-96069370	GM12872	blood:	n/a	n/a
22	CTCF	chr2:96079480-96079630	HepG2	liver:	n/a	n/a
23	CTCF	chr2:96079900-96080050	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr2:96069120-96069270	HRE	kidney:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
25	CTCF	chr2:96069080-96069230	GM12866	blood:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
26	CTCF	chr2:96070571-96070740	HepG2	liver:	n/a	chr2:96070639-96070652
27	CTCF	chr2:96069120-96069270	BJ	skin:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
28	CTCF	chr2:96079795-96080060	GM10266	blood:	n/a	n/a
29	CTCF	chr2:96079778-96080101	ECC-1	luminal epithelium:	n/a	n/a
30	CTCF	chr2:96069080-96069230	GM12871	blood:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
31	CTCF	chr2:96069100-96069250	AG04450	lung:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
32	CTCF	chr2:96079880-96080030	GM12872	blood:	n/a	n/a
33	CTCF	chr2:96079595-96079631	GM19238	blood:	n/a	n/a
34	CTCF	chr2:96069140-96069290	HPAF	blood vessel:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
35	CTCF	chr2:96079860-96080010	AoAF	blood vessel:	n/a	n/a
36	CTCF	chr2:96079860-96080010	HCPEpiC	choroid plexus:	n/a	n/a
37	CTCF	chr2:96070563-96070700	K562	blood:	n/a	chr2:96070639-96070652
38	CTCF	chr2:96069080-96069230	HepG2	liver:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
39	CTCF	chr2:96079761-96080062	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr2:96079800-96080171	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:96079460-96079610	AG04450	lung:	n/a	n/a
42	CTCF	chr2:96068909-96069331	A549	lung:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
43	CTCF	chr2:96069100-96069250	WI-38	lung:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
44	CTCF	chr2:96069100-96069250	NB4	blood:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
45	CTCF	chr2:96079920-96080070	HEK293	kidney:	n/a	n/a
46	CTCF	chr2:96079791-96080065	GM12878	blood:	n/a	n/a
47	CTCF	chr2:96079500-96079650	AG10803	skin:	n/a	n/a
48	CTCF	chr2:96069055-96069332	K562	blood:	n/a	chr2:96069183-96069196 chr2:96069181-96069197
49	CTCF	chr2:96079707-96080100	K562	blood:	n/a	n/a
50	CTCF	chr2:96079730-96080055	T-47D	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:96078823-96078873	NH-A	brain:	n/a
2	chr2:96071494-96071544	HNPCEpiC	eye:	n/a
3	chr2:96071494-96071544	NT2-D1	testis:	n/a
4	chr2:96078823-96078873	AG04450	lung:	fetal
5	chr2:96071494-96071544	SKMC	muscle:	n/a
6	chr2:96071494-96071544	ProgFib	skin:	n/a
7	chr2:96071494-96071544	HCM	heart:	n/a
8	chr2:96071494-96071544	HAEpiC	amniotic membrane:	n/a
9	chr2:96071494-96071544	MCF10A-Er-Src	breast:	n/a
10	chr2:96078823-96078873	BJ	skin:	n/a
11	chr2:96071494-96071544	GM12891	blood:	n/a
12	chr2:96071494-96071544	HUVEC	blood vessel:	n/a
13	chr2:96071494-96071544	HIPEpiC	eye:	n/a
14	chr2:96071494-96071544	Jurkat	blood:	n/a
15	chr2:96078823-96078873	NT2-D1	testis:	n/a
16	chr2:96071494-96071544	AG04450	lung:	fetal
17	chr2:96071494-96071544	IMR90	lung:	fetal
18	chr2:96071494-96071544	BJ	skin:	n/a
19	chr2:96078823-96078873	HPAEpiC	pulmonary alveolar:	n/a
20	chr2:96078823-96078873	H1-hESC	embryonic stem cell:	embryo
21	chr2:96071494-96071544	PANC-1	pancreas:	n/a
22	chr2:96078823-96078873	HRCEpiC	kidney:	n/a
23	chr2:96078823-96078873	GM06990	blood:	n/a
24	chr2:96071494-96071544	HRCEpiC	kidney:	n/a
25	chr2:96071494-96071544	AG10803	skin:	n/a
26	chr2:96078823-96078873	HAEpiC	amniotic membrane:	n/a
27	chr2:96078823-96078873	Caco-2	colon:	n/a
28	chr2:96078823-96078873	RPTEC	kidney:	n/a
29	chr2:96071494-96071544	HPAEpiC	pulmonary alveolar:	n/a
30	chr2:96071494-96071544	NH-A	brain:	n/a
31	chr2:96078823-96078873	GM12892	blood:	n/a
32	chr2:96078823-96078873	HRE	kidney:	n/a
33	chr2:96078823-96078873	GM12891	blood:	n/a
34	chr2:96071494-96071544	Caco-2	colon:	n/a
35	chr2:96078823-96078873	HCM	heart:	n/a
36	chr2:96078823-96078873	HEEpiC	esophagus:	n/a
37	chr2:96078823-96078873	ECC-1	luminal epithelium:	n/a
38	chr2:96071494-96071544	AG09309	skin:	n/a
39	chr2:96071494-96071544	HEK293	kidney:	embryo
40	chr2:96071494-96071544	AG09319	gingival:	n/a
41	chr2:96071494-96071544	PrEC	prostate:	n/a
42	chr2:96071494-96071544	ECC-1	luminal epithelium:	n/a
43	chr2:96078823-96078873	SK-N-SH	brain:	n/a
44	chr2:96078823-96078873	HIPEpiC	eye:	n/a
45	chr2:96078823-96078873	HepG2	liver:	n/a
46	chr2:96078823-96078873	HL-60	blood:	n/a
47	chr2:96071494-96071544	AoSMC	blood vessel:	n/a
48	chr2:96071494-96071544	Hepatocyte	liver:	n/a
49	chr2:96071494-96071544	SK-N-SH_RA	brain:	n/a
50	chr2:96071494-96071544	PFSK-1	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:96075502..96078062-chr2:96080565..96082450,2	K562	blood:
2	chr2:96067874..96069993-chr2:96073132..96075556,2	MCF-7	breast:
3	chr2:96075502..96078062-chr2:96080565..96082450,2	K562	blood:
4	chr2:96066494..96069918-chr2:96073464..96075221,3	K562	blood:
5	chr2:96074947..96078062-chr2:96079225..96082450,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNIP3-4	chr2:96080756-96082345	NONHSAT072486

No data

Variant related genes	Relation type
FAHD2A	TF binding region
ENSG00000248821	TF binding region
FAHD2A	CpG island
ENSG00000248821	CpG island
ENSG00000248821	chromatin interactions
ENSG00000115042	chromatin interactions

Extended variants
information (count: 472 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536396008	chr2:96069209-96069210	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs377588969	chr2:96069217-96069218	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs370585667	chr2:96069228-96069229	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs573029442	chr2:96069319-96069320	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs545235036	chr2:96069336-96069337	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs534492791	chr2:96069338-96069339	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147005868	chr2:96069375-96069376	Active TSS Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs116625493	chr2:96069495-96069496	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551058260	chr2:96069552-96069553	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs148402966	chr2:96069554-96069555	Flanking Active TSS Active TSS Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs530131054	chr2:96069606-96069607	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs546641690	chr2:96069615-96069616	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs560220996	chr2:96069617-96069618	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs532531682	chr2:96069643-96069644	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs569381222	chr2:96069672-96069673	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs186178520	chr2:96069681-96069682	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569509032	chr2:96069760-96069761	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs531943365	chr2:96069843-96069844	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs201278222	chr2:96069889-96069890	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs567199415	chr2:96069919-96069920	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs536258301	chr2:96069951-96069952	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs553065179	chr2:96069965-96069966	Weak transcription Active TSS Enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs113250091	chr2:96070043-96070044	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs368946584	chr2:96070078-96070079	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs566588995	chr2:96070098-96070099	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs538810876	chr2:96070106-96070107	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs192067644	chr2:96070135-96070136	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs113373060	chr2:96070145-96070146	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs544225850	chr2:96070165-96070166	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs554851040	chr2:96070202-96070203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs112363885	chr2:96070203-96070204	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75072794	chr2:96070231-96070232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs540247013	chr2:96070232-96070233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560182845	chr2:96070347-96070348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs532495703	chr2:96070399-96070400	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150641355	chr2:96070415-96070416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186845523	chr2:96070424-96070425	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs532031256	chr2:96070462-96070463	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs548555788	chr2:96070463-96070464	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs111999984	chr2:96070534-96070535	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs568780888	chr2:96070589-96070590	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs529682423	chr2:96070612-96070613	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs546642021	chr2:96070613-96070614	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs573475343	chr2:96070617-96070618	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs538390498	chr2:96070725-96070726	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs558714340	chr2:96070762-96070763	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs568912606	chr2:96070764-96070765	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs191228270	chr2:96070799-96070800	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs554532946	chr2:96070800-96070801	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs574412347	chr2:96070888-96070889	Weak transcription Enhancers Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:49)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	17483303	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myxofibrosarcoma	16751306	CNVD
Breast cancer	16272173	CNVD
Ovarian cancer	21781307	CNVD
Lung cancer	18438408	CNVD
Mowat-Wilson syndrome	21572526	CNVD
Disorders of sex development	21048976	CNVD
epilepsy	18472482	CNVD
Ewing''s sarcoma	17952124	CNVD
Neuroblastoma	18574593	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21509527	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD

Chromatin state (count:538 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:96067200-96069200	Active TSS	HSMM	muscle
2	chr2:96067400-96069200	Active TSS	NHDF-Ad	bronchial
3	chr2:96067400-96069400	Active TSS	Pancreatic Islets	Pancreatic Islet
4	chr2:96067400-96069600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr2:96067600-96069200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr2:96067600-96069200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
7	chr2:96067600-96069200	Active TSS	Fetal Intestine Large	intestine
8	chr2:96067600-96069400	Active TSS	HUES64 Cell Line	embryonic stem cell
9	chr2:96067600-96069600	Active TSS	H9 Cell Line	embryonic stem cell
10	chr2:96067600-96069600	Active TSS	Fetal Kidney	kidney
11	chr2:96067800-96069200	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
12	chr2:96067800-96069200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
13	chr2:96067800-96069200	Active TSS	Breast Myoepithelial Primary Cells	Breast
14	chr2:96067800-96069200	Active TSS	Primary T helper naive cells from peripheral blood	blood
15	chr2:96067800-96069200	Active TSS	Primary T killer memory cells from peripheral blood	blood
16	chr2:96067800-96069200	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr2:96067800-96069200	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr2:96067800-96069200	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
19	chr2:96067800-96069200	Active TSS	Brain Angular Gyrus	brain
20	chr2:96067800-96069200	Active TSS	Brain Anterior Caudate	brain
21	chr2:96067800-96069200	Active TSS	Brain Cingulate Gyrus	brain
22	chr2:96067800-96069200	Active TSS	Brain Substantia Nigra	brain
23	chr2:96067800-96069200	Active TSS	Duodenum Smooth Muscle	Duodenum
24	chr2:96067800-96069200	Active TSS	Fetal Brain Female	brain
25	chr2:96067800-96069200	Active TSS	Fetal Lung	lung
26	chr2:96067800-96069200	Active TSS	Fetal Thymus	thymus
27	chr2:96067800-96069200	Active TSS	Gastric	stomach
28	chr2:96067800-96069200	Active TSS	Ovary	ovary
29	chr2:96067800-96069200	Active TSS	Placenta Amnion	Placenta Amnion
30	chr2:96067800-96069200	Active TSS	Psoas Muscle	Psoas
31	chr2:96067800-96069200	Active TSS	Small Intestine	intestine
32	chr2:96067800-96069200	Active TSS	GM12878-XiMat	blood
33	chr2:96067800-96069200	Active TSS	Hela-S3	cervix
34	chr2:96067800-96069200	Active TSS	K562	blood
35	chr2:96067800-96069200	Active TSS	NHLF	lung
36	chr2:96067800-96069400	Active TSS	ES-I3 Cell Line	embryonic stem cell
37	chr2:96067800-96069400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr2:96067800-96069400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr2:96067800-96069400	Active TSS	Brain Hippocampus Middle	brain
40	chr2:96067800-96069400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
41	chr2:96067800-96069400	Active TSS	Colon Smooth Muscle	Colon
42	chr2:96067800-96069400	Active TSS	Fetal Intestine Small	intestine
43	chr2:96067800-96069400	Active TSS	Left Ventricle	heart
44	chr2:96067800-96069400	Active TSS	Right Atrium	heart
45	chr2:96067800-96069400	Active TSS	A549	lung
46	chr2:96067800-96069600	Active TSS	H1 Cell Line	embryonic stem cell
47	chr2:96067800-96069600	Active TSS	iPS-15b Cell Line	embryonic stem cell
48	chr2:96067800-96069600	Active TSS	iPS-18 Cell Line	embryonic stem cell
49	chr2:96067800-96069600	Active TSS	iPS-20b Cell Line	embryonic stem cell
50	chr2:96067800-96069600	Active TSS	Brain Germinal Matrix	brain

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