Variant report

Variant	nsv1004993
Chromosome Location	chr1:245940334-245960376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:275)
CpG islands
(count:61)
Chromatin interactive
region (count:17)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:275 , 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	ARID3A	chr1:245955072-245955365	K562	blood:	n/a	n/a
2	ATF1	chr1:245955020-245955416	K562	blood:	n/a	n/a
3	BACH1	chr1:245955280-245955283	K562	blood:	n/a	n/a
4	BHLHE40	chr1:245955032-245955320	K562	blood:	n/a	n/a
5	CCNT2	chr1:245954882-245955315	K562	blood:	n/a	n/a
6	CEBPB	chr1:245953685-245953732	A549	lung:	n/a	n/a
7	CEBPB	chr1:245951825-245951972	K562	blood:	n/a	chr1:245951865-245951876
8	CEBPB	chr1:245951629-245952071	IMR90	lung:	n/a	chr1:245951865-245951876
9	CEBPB	chr1:245951730-245951984	Hela-S3	cervix:	n/a	chr1:245951865-245951876
10	CEBPB	chr1:245951771-245951970	A549	lung:	n/a	chr1:245951865-245951876
11	CEBPB	chr1:245951786-245952007	HepG2	liver:	n/a	chr1:245951865-245951876
12	CEBPD	chr1:245955011-245955412	K562	blood:	n/a	n/a
13	CHD2	chr1:245955233-245955257	K562	blood:	n/a	n/a
14	CTCF	chr1:245943240-245943390	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr1:245943140-245943290	GM12875	blood:	n/a	n/a
16	CTCF	chr1:245943160-245943310	Hela-S3	cervix:	n/a	n/a
17	CTCF	chr1:245950520-245950670	AG10803	skin:	n/a	n/a
18	CTCF	chr1:245943200-245943350	HFF-Myc	foreskin:	n/a	n/a
19	CTCF	chr1:245943400-245943550	GM12872	blood:	n/a	n/a
20	CTCF	chr1:245943200-245943350	HAc	cerebellar:	n/a	n/a
21	CTCF	chr1:245943160-245943310	BE2_C	brain:	n/a	n/a
22	CTCF	chr1:245943220-245943370	GM12866	blood:	n/a	n/a
23	CTCF	chr1:245943180-245943330	HPF	lung:	n/a	n/a
24	CTCF	chr1:245943200-245943350	HA-sp	spinal cord:	n/a	n/a
25	CTCF	chr1:245943320-245943470	GM12871	blood:	n/a	n/a
26	CTCF	chr1:245943200-245943350	AG09309	skin:	n/a	n/a
27	CTCF	chr1:245950500-245950650	HMF	breast:	n/a	n/a
28	CTCF	chr1:245943252-245943313	Gliobla	brain:	n/a	n/a
29	CTCF	chr1:245943220-245943370	GM12867	blood:	n/a	n/a
30	CTCF	chr1:245943180-245943330	BJ	skin:	n/a	n/a
31	CTCF	chr1:245950520-245950670	AG09319	gingival:	n/a	n/a
32	CTCF	chr1:245943161-245943432	K562	blood:	n/a	n/a
33	CTCF	chr1:245943080-245943230	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr1:245943220-245943370	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr1:245943160-245943310	GM12867	blood:	n/a	n/a
36	CTCF	chr1:245943186-245943417	K562	blood:	n/a	n/a
37	CTCF	chr1:245943100-245943250	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr1:245943160-245943310	GM12868	blood:	n/a	n/a
39	CTCF	chr1:245943220-245943370	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr1:245943280-245943430	BE2_C	brain:	n/a	n/a
41	CTCF	chr1:245943200-245943350	GM12878	blood:	n/a	n/a
42	CTCF	chr1:245943200-245943350	HCT-116	colon:	n/a	n/a
43	CTCF	chr1:245943140-245943410	AG04450	lung:	n/a	n/a
44	CTCF	chr1:245943260-245943410	HVMF	connective:	n/a	n/a
45	CTCF	chr1:245943278-245943284	K562	blood:	n/a	n/a
46	CTCF	chr1:245950500-245950650	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr1:245943200-245943350	NHEK	skin:	n/a	n/a
48	CTCF	chr1:245950480-245950630	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr1:245943185-245943507	K562	blood:	n/a	n/a
50	CTCF	chr1:245943180-245943330	AG09309	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:245951603-245951653	H1-hESC	embryonic stem cell:	embryo
2	chr1:245951603-245951653	PFSK-1	brain:	n/a
3	chr1:245951603-245951653	AG10803	skin:	n/a
4	chr1:245951603-245951653	HepG2	liver:	n/a
5	chr1:245951603-245951653	GM12891	blood:	n/a
6	chr1:245951603-245951653	NH-A	brain:	n/a
7	chr1:245951603-245951653	HL-60	blood:	n/a
8	chr1:245951603-245951653	NB4	blood:	n/a
9	chr1:245951603-245951653	NHDF-neo	bronchial:	n/a
10	chr1:245951603-245951653	HCM	heart:	n/a
11	chr1:245951603-245951653	ProgFib	skin:	n/a
12	chr1:245951603-245951653	HMEC	breast:	n/a
13	chr1:245951603-245951653	Hela-S3	cervix:	n/a
14	chr1:245951603-245951653	AG09319	gingival:	n/a
15	chr1:245951603-245951653	SK-N-SH	brain:	n/a
16	chr1:245951603-245951653	NHBE	bronchial:	n/a
17	chr1:245951603-245951653	Caco-2	colon:	n/a
18	chr1:245951603-245951653	SKMC	muscle:	n/a
19	chr1:245951603-245951653	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:245951603-245951653	AG04450	lung:	fetal
21	chr1:245951603-245951653	HRCEpiC	kidney:	n/a
22	chr1:245951603-245951653	HUVEC	blood vessel:	n/a
23	chr1:245951603-245951653	MCF-7	breast:	n/a
24	chr1:245951603-245951653	HAEpiC	amniotic membrane:	n/a
25	chr1:245951603-245951653	AG04449	skin:	fetal
26	chr1:245951603-245951653	ovcar-3	ovarian:	n/a
27	chr1:245951603-245951653	A549	lung:	n/a
28	chr1:245951603-245951653	CMK	blood:	n/a
29	chr1:245951603-245951653	AoSMC	blood vessel:	n/a
30	chr1:245951603-245951653	HCPEpiC	choroid plexus:	n/a
31	chr1:245951603-245951653	U87	brain:	n/a
32	chr1:245951603-245951653	SK-N-SH_RA	brain:	n/a
33	chr1:245951603-245951653	GM19239	blood:	n/a
34	chr1:245951603-245951653	AG09309	skin:	n/a
35	chr1:245951603-245951653	ECC-1	luminal epithelium:	n/a
36	chr1:245951603-245951653	Jurkat	blood:	n/a
37	chr1:245951603-245951653	SK-N-MC	brain:	n/a
38	chr1:245951603-245951653	BJ	skin:	n/a
39	chr1:245951603-245951653	PANC-1	pancreas:	n/a
40	chr1:245951603-245951653	MCF10A-Er-Src	breast:	n/a
41	chr1:245951603-245951653	HCT-116	colon:	n/a
42	chr1:245951603-245951653	IMR90	lung:	fetal
43	chr1:245951603-245951653	GM06990	blood:	n/a
44	chr1:245951603-245951653	HNPCEpiC	eye:	n/a
45	chr1:245951603-245951653	PrEC	prostate:	n/a
46	chr1:245951603-245951653	HCF	heart:	n/a
47	chr1:245951603-245951653	HRE	kidney:	n/a
48	chr1:245951603-245951653	T-47D	breast:	n/a
49	chr1:245951603-245951653	GM12892	blood:	n/a
50	chr1:245951603-245951653	HIPEpiC	eye:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:245958486..245963819-chr1:245964384..245971753,7	K562	blood:
2	chr1:245941838..245944477-chr1:245947210..245948846,2	K562	blood:
3	chr1:245936756..245938945-chr1:245939656..245941658,2	K562	blood:
4	chr1:245945508..245948096-chr1:245953816..245955948,2	K562	blood:
5	chr1:245945508..245948096-chr1:245953816..245955948,2	K562	blood:
6	chr1:245941838..245944477-chr1:245947210..245948846,2	K562	blood:
7	chr1:245955103..245956955-chr1:245958700..245960515,2	K562	blood:
8	chr1:245951618..245953309-chr1:245958788..245960610,2	K562	blood:
9	chr1:245946341..245948096-chr1:245954094..245955948,2	K562	blood:
10	chr1:245939310..245941054-chr1:245942371..245944606,2	K562	blood:
11	chr1:245939310..245941054-chr1:245942371..245944606,2	K562	blood:
12	chr1:245946341..245948096-chr1:245954094..245955948,2	K562	blood:
13	chr1:245955103..245956955-chr1:245958700..245960515,2	K562	blood:
14	chr1:245953135..245953939-chr22:40742433..40743017,2	HCT-116	colon:
15	chr1:245942970..245944727-chr1:245958488..245960001,2	K562	blood:
16	chr1:245949980..245953716-chr1:245955900..245958443,3	K562	blood:
17	chr1:245942970..245944727-chr1:245958488..245960001,2	K562	blood:

No data

Variant related genes	Relation type
SMYD3	TF binding region
SMYD3	CpG island
ENSG00000185420	chromatin interactions
ENSG00000239900	chromatin interactions

Extended variants
information (count: 824 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:824 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6687221	chr1:245940334-245940335	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs183630340	chr1:245940400-245940401	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs187565941	chr1:245940411-245940412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs371083825	chr1:245940420-245940421	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138990689	chr1:245940460-245940461	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs539385185	chr1:245940494-245940495	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs559178097	chr1:245940547-245940548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs201509023	chr1:245940557-245940558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs143016709	chr1:245940622-245940623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575658289	chr1:245940643-245940644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs538790533	chr1:245940710-245940711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs193244449	chr1:245940718-245940719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs574948063	chr1:245940724-245940725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185743096	chr1:245940729-245940730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560779493	chr1:245940848-245940849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577609362	chr1:245940864-245940865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs546550010	chr1:245940865-245940866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190159384	chr1:245940877-245940878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs531757061	chr1:245940926-245940927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548637540	chr1:245940958-245940959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181864467	chr1:245941000-245941001	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs527443892	chr1:245941007-245941008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs150899189	chr1:245941026-245941027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs139429159	chr1:245941100-245941101	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149612302	chr1:245941111-245941112	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs112626645	chr1:245941151-245941152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370492768	chr1:245941165-245941166	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs7523473	chr1:245941175-245941176	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs552755370	chr1:245941202-245941203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116928599	chr1:245941205-245941206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs7536011	chr1:245941269-245941270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570633547	chr1:245941270-245941271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs144363059	chr1:245941274-245941275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs532011716	chr1:245941285-245941286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs79500431	chr1:245941318-245941319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs10924334	chr1:245941394-245941395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572038149	chr1:245941421-245941422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2817486	chr1:245941462-245941463	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs2817485	chr1:245941607-245941608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs12043524	chr1:245941659-245941660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184039079	chr1:245941664-245941665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs563199471	chr1:245941681-245941682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113114667	chr1:245941684-245941685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs2185374	chr1:245941685-245941686	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs76716539	chr1:245941694-245941695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs35258243	chr1:245941697-245941698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs188772158	chr1:245941719-245941720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs114996531	chr1:245941720-245941721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547896617	chr1:245941721-245941722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563922010	chr1:245941769-245941770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Liposarcoma	21253554	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	20729466	CNVD
Testicular germ cell tumor	18059402	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Basal cell lymphoma	17170743	CNVD
Basal cell lymphoma	17053054	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164920	CNVD
Cancer	17060936	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16616336	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	22291905	CNVD
Myelofibrosis	22110671	CNVD
Disease	21936942	CNVD
laryngomalacia	21936942	CNVD
GLUT3 deficiency syndrome	20509907	CNVD
Developmental delay	21373258	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Developmental delay	19490664	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Cutaneous malignant melanoma	18794153	CNVD
Astrocytoma	17934521	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Breast cancer	20409316	CNVD
Fibroblasts	17951408	CNVD
Lung cancer	17951408	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:245911800-245943600	Weak transcription	Dnd41	blood
2	chr1:245931200-245943600	Weak transcription	Aorta	Aorta
3	chr1:245931200-245948800	Weak transcription	Gastric	stomach
4	chr1:245931800-245942400	Weak transcription	HepG2	liver
5	chr1:245932000-245966200	Weak transcription	Primary T cells from cord blood	blood
6	chr1:245935800-245952000	Weak transcription	K562	blood
7	chr1:245936200-245943400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:245936200-245950600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:245936600-245941000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:245936600-245950400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr1:245939800-245940400	Enhancers	Brain Germinal Matrix	brain
12	chr1:245939800-245940600	Enhancers	Fetal Heart	heart
13	chr1:245939800-245940600	Enhancers	Fetal Kidney	kidney
14	chr1:245940000-245940400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr1:245940000-245940400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr1:245940600-245945600	Weak transcription	Fetal Heart	heart
17	chr1:245941000-245941200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
18	chr1:245943400-245943800	ZNF genes & repeats	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr1:245943800-245951000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr1:245945400-245945800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr1:245945600-245946800	Enhancers	Fetal Heart	heart
22	chr1:245946600-245951200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr1:245946800-245950800	Weak transcription	Fetal Heart	heart
24	chr1:245948800-245949000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:245948800-245949000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr1:245948800-245949200	Enhancers	Gastric	stomach
27	chr1:245949000-245949200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr1:245949000-245950600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr1:245949200-245961400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr1:245949200-245999600	Weak transcription	Gastric	stomach
31	chr1:245949800-245955000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:245950200-245950400	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr1:245950400-245952400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr1:245950600-245951200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:245950600-245951200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr1:245950600-245951200	Enhancers	NHDF-Ad	bronchial
37	chr1:245950600-245951200	Enhancers	NHLF	lung
38	chr1:245950600-245952200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr1:245950800-245951200	Enhancers	Fetal Heart	heart
40	chr1:245950800-245952000	Weak transcription	HepG2	liver
41	chr1:245951000-245951200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr1:245951000-245951200	Enhancers	Muscle Satellite Cultured Cells	--
43	chr1:245951000-245951200	Enhancers	Osteobl	bone
44	chr1:245951000-245952200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr1:245951000-245954600	Enhancers	NH-A	brain
46	chr1:245951200-245951400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr1:245951200-245951600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr1:245951200-245951600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr1:245951200-245951600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
50	chr1:245951200-245951600	Flanking Active TSS	NHDF-Ad	bronchial

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links