Variant report

Variant	nsv999833
Chromosome Location	chr1:210604734-210620211
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:159)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:159 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr1:210612405-210612891	A549	lung:	n/a	n/a
2	ATF3	chr1:210612457-210612901	A549	lung:	n/a	n/a
3	BATF	chr1:210619807-210620273	GM12878	blood:	n/a	n/a
4	BHLHE40	chr1:210619822-210620085	GM12878	blood:	n/a	n/a
5	CEBPB	chr1:210612073-210612902	A549	lung:	n/a	n/a
6	CEBPB	chr1:210612131-210613087	IMR90	lung:	n/a	n/a
7	CEBPB	chr1:210618865-210619155	MCF-7	breast:	n/a	n/a
8	CEBPB	chr1:210618825-210619192	MCF-7	breast:	n/a	n/a
9	CREB1	chr1:210612249-210612449	A549	lung:	n/a	n/a
10	CREB1	chr1:210612246-210612516	A549	lung:	n/a	n/a
11	CTCF	chr1:210614360-210614510	AG04449	skin:	n/a	n/a
12	CTCF	chr1:210614340-210614490	GM12867	blood:	n/a	n/a
13	CTCF	chr1:210614344-210614499	GM12878	blood:	n/a	n/a
14	CTCF	chr1:210614405-210614497	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:210614401-210614509	Gliobla	brain:	n/a	n/a
16	CTCF	chr1:210614420-210614492	K562	blood:	n/a	n/a
17	CTCF	chr1:210614389-210614539	MCF-7	breast:	n/a	chr1:210614505-210614513
18	CTCF	chr1:210614300-210614450	GM12873	blood:	n/a	n/a
19	CTCF	chr1:210614391-210614489	MCF-7	breast:	n/a	n/a
20	CTCF	chr1:210614391-210614535	A549	lung:	n/a	chr1:210614505-210614513
21	CTCF	chr1:210614380-210614530	WERI-Rb-1	eye:	n/a	chr1:210614505-210614513
22	CTCF	chr1:210614400-210614550	A549	lung:	n/a	chr1:210614505-210614513
23	CTCF	chr1:210614398-210614499	ProgFib	skin:	n/a	n/a
24	CTCF	chr1:210614424-210614488	MCF-7	breast:	n/a	n/a
25	CTCF	chr1:210614395-210614527	MCF-7	breast:	n/a	chr1:210614505-210614513
26	CTCF	chr1:210614472-210614496	GM19239	blood:	n/a	n/a
27	CTCF	chr1:210614420-210614570	AG04449	skin:	n/a	chr1:210614505-210614513
28	CTCF	chr1:210614395-210614533	NHEK	skin:	n/a	chr1:210614505-210614513
29	E2F4	chr1:210614879-210614960	MCF10A-Er-Src	breast:	n/a	n/a
30	EBF1	chr1:210614376-210614877	GM12878	blood:	n/a	chr1:210614646-210614657
31	EBF1	chr1:210614442-210614796	GM12878	blood:	n/a	chr1:210614646-210614657
32	EBF1	chr1:210612804-210613088	GM12878	blood:	n/a	chr1:210612975-210612986
33	EBF1	chr1:210612767-210614008	GM12878	blood:	n/a	chr1:210612975-210612986
34	EP300	chr1:210611954-210613174	A549	lung:	n/a	n/a
35	EP300	chr1:210612135-210613075	A549	lung:	n/a	n/a
36	EP300	chr1:210612017-210613121	SK-N-SH	brain:	n/a	n/a
37	FOS	chr1:210619796-210620080	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr1:210619857-210620092	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr1:210619012-210619019	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr1:210619867-210620070	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr1:210619779-210620090	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr1:210612276-210612788	HUVEC	blood vessel:	n/a	n/a
43	FOS	chr1:210612291-210612413	MCF10A-Er-Src	breast:	n/a	n/a
44	FOSL2	chr1:210612173-210612801	A549	lung:	n/a	n/a
45	FOSL2	chr1:210612155-210613060	SK-N-SH	brain:	n/a	n/a
46	FOSL2	chr1:210612134-210612848	SK-N-SH	brain:	n/a	n/a
47	FOSL2	chr1:210612077-210613020	A549	lung:	n/a	n/a
48	FOSL2	chr1:210619703-210620075	HepG2	liver:	n/a	n/a
49	FOXA1	chr1:210614383-210614700	T-47D	breast:	n/a	n/a
50	FOXA1	chr1:210618889-210619144	T-47D	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:210612391-210612441	ovcar-3	ovarian:	n/a
2	chr1:210607796-210607846	GM12891	blood:	n/a
3	chr1:210612391-210612441	HUVEC	blood vessel:	n/a
4	chr1:210613691-210613741	BJ	skin:	n/a
5	chr1:210612391-210612441	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:210613691-210613741	HRE	kidney:	n/a
7	chr1:210607796-210607846	T-47D	breast:	n/a
8	chr1:210613691-210613741	PFSK-1	brain:	n/a
9	chr1:210612391-210612441	HMEC	breast:	n/a
10	chr1:210612391-210612441	HCM	heart:	n/a
11	chr1:210607796-210607846	PFSK-1	brain:	n/a
12	chr1:210612391-210612441	IMR90	lung:	fetal
13	chr1:210612391-210612441	AG09319	gingival:	n/a
14	chr1:210613691-210613741	HEEpiC	esophagus:	n/a
15	chr1:210607796-210607846	GM12878	blood:	n/a
16	chr1:210607796-210607846	HepG2	liver:	n/a
17	chr1:210612391-210612441	SAEC	small airway:	n/a
18	chr1:210607796-210607846	HNPCEpiC	eye:	n/a
19	chr1:210612391-210612441	HCF	heart:	n/a
20	chr1:210612391-210612441	HRCEpiC	kidney:	n/a
21	chr1:210607796-210607846	HRCEpiC	kidney:	n/a
22	chr1:210612391-210612441	NB4	blood:	n/a
23	chr1:210613691-210613741	HCT-116	colon:	n/a
24	chr1:210613691-210613741	Hepatocyte	liver:	n/a
25	chr1:210612391-210612441	NHDF-neo	bronchial:	n/a
26	chr1:210613691-210613741	HPAEpiC	pulmonary alveolar:	n/a
27	chr1:210613691-210613741	GM12892	blood:	n/a
28	chr1:210607796-210607846	GM12892	blood:	n/a
29	chr1:210612391-210612441	GM12892	blood:	n/a
30	chr1:210612391-210612441	HAEpiC	amniotic membrane:	n/a
31	chr1:210613691-210613741	Hela-S3	cervix:	n/a
32	chr1:210613691-210613741	HAEpiC	amniotic membrane:	n/a
33	chr1:210612391-210612441	MCF10A-Er-Src	breast:	n/a
34	chr1:210607796-210607846	HUVEC	blood vessel:	n/a
35	chr1:210607796-210607846	AG04450	lung:	fetal
36	chr1:210613691-210613741	MCF-7	breast:	n/a
37	chr1:210612391-210612441	Caco-2	colon:	n/a
38	chr1:210613691-210613741	HL-60	blood:	n/a
39	chr1:210613691-210613741	T-47D	breast:	n/a
40	chr1:210607796-210607846	SAEC	small airway:	n/a
41	chr1:210607796-210607846	BE2_C	brain:	n/a
42	chr1:210613691-210613741	AG10803	skin:	n/a
43	chr1:210607796-210607846	Hepatocyte	liver:	n/a
44	chr1:210613691-210613741	SKMC	muscle:	n/a
45	chr1:210607796-210607846	Hela-S3	cervix:	n/a
46	chr1:210613691-210613741	PANC-1	pancreas:	n/a
47	chr1:210612391-210612441	RPTEC	kidney:	n/a
48	chr1:210607796-210607846	ProgFib	skin:	n/a
49	chr1:210613691-210613741	Caco-2	colon:	n/a
50	chr1:210612391-210612441	CMK	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:210545855..210547911-chr1:210612937..210615260,3	K562	blood:
2	chr1:210612929..210615850-chr1:210617890..210620157,2	K562	blood:
3	chr1:210603462..210605610-chr1:210606812..210609556,2	MCF-7	breast:
4	chr1:210612929..210615850-chr1:210617890..210620157,2	K562	blood:
5	chr1:210545823..210547818-chr1:210606420..210608728,2	K562	blood:
6	chr1:210545786..210547818-chr1:210606420..210608180,2	K562	blood:
7	chr1:210618870..210621785-chr1:211306135..211307908,2	MCF-7	breast:
8	chr1:210617470..210620137-chr1:211308701..211310289,2	MCF-7	breast:
9	chr1:210603462..210605610-chr1:210606812..210609556,2	MCF-7	breast:
10	chr1:210545308..210548162-chr1:210603373..210605975,2	MCF-7	breast:
11	chr1:210545794..210547749-chr1:210620055..210622714,2	MCF-7	breast:

No data

Variant related genes	Relation type
HHAT	TF binding region
HHAT	CpG island
ENSG00000234233	chromatin interactions
ENSG00000200972	chromatin interactions
ENSG00000143473	chromatin interactions

Extended variants
information (count: 618 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142463139	chr1:210604734-210604735	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs144712691	chr1:210604736-210604737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs35213283	chr1:210604855-210604856	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs138447423	chr1:210604862-210604863	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs533465584	chr1:210604889-210604890	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs149621556	chr1:210604919-210604920	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs570133611	chr1:210604933-210604934	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs144328574	chr1:210604968-210604969	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs555574701	chr1:210604995-210604996	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs567764324	chr1:210605025-210605026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs188206378	chr1:210605056-210605057	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs148801193	chr1:210605057-210605058	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs143286081	chr1:210605070-210605071	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs12723999	chr1:210605079-210605080	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs147458134	chr1:210605095-210605096	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs6656493	chr1:210605104-210605105	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs543650798	chr1:210605109-210605110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs561402283	chr1:210605116-210605117	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs573415132	chr1:210605179-210605180	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs540595319	chr1:210605245-210605246	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541298626	chr1:210605258-210605259	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs74156158	chr1:210605274-210605275	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs577799386	chr1:210605284-210605285	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs11119495	chr1:210605289-210605290	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs573843869	chr1:210605336-210605337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs564205132	chr1:210605380-210605381	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs74976020	chr1:210605403-210605404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556401839	chr1:210605434-210605435	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs530959177	chr1:210605442-210605443	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4845025	chr1:210605563-210605564	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs145345668	chr1:210605589-210605590	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs535145751	chr1:210605658-210605659	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs11119496	chr1:210605675-210605676	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs571653555	chr1:210605676-210605677	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs113801360	chr1:210605762-210605763	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs528916608	chr1:210605774-210605775	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs151075743	chr1:210605845-210605846	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs115835530	chr1:210605846-210605847	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs12117900	chr1:210605890-210605891	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs12749929	chr1:210605899-210605900	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs12136541	chr1:210605902-210605903	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs573526860	chr1:210605909-210605910	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs77330000	chr1:210605957-210605958	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs12117930	chr1:210605960-210605961	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs376416702	chr1:210605961-210605962	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530334473	chr1:210606007-210606008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs550023135	chr1:210606025-210606026	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs563558284	chr1:210606064-210606065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs532541262	chr1:210606085-210606086	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs551090556	chr1:210606107-210606108	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	17443227	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
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
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Breast cancer	21509527	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17393978	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Trisomy 5 syndrome	21098271	CNVD
Urothelial carcinoma	21177765	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chordoma	18071362	CNVD
Macular degeneration	22558131	CNVD
Alzheimer''s disease	21403675	CNVD
Multiple myeloma	16461302	CNVD
van der Woude syndrome	22470819	CNVD
van der Woude syndrome	20818247	CNVD
T-cell lymphomas	19863542	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	17060936	CNVD
Atypical hemolytic uremic syndrome	19861685	CNVD
Hepatocellular carcinoma	18803288	CNVD
Urothelial tumor	18831757	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:199 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210567400-210617200	Weak transcription	Left Ventricle	heart
2	chr1:210571400-210641000	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr1:210586400-210610800	Weak transcription	Aorta	Aorta
4	chr1:210592000-210609400	Weak transcription	Ovary	ovary
5	chr1:210592800-210625000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:210601000-210607600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
7	chr1:210602400-210613600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr1:210604200-210610000	Weak transcription	HSMM	muscle
9	chr1:210604600-210607200	Weak transcription	HSMMtube	muscle
10	chr1:210605600-210605800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr1:210605600-210608000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr1:210605800-210606200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr1:210605800-210606800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr1:210606600-210607400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr1:210606600-210608000	Enhancers	H1 Cell Line	embryonic stem cell
16	chr1:210606600-210608000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr1:210606800-210608000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr1:210606800-210608000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr1:210606800-210608000	Enhancers	iPS-15b Cell Line	embryonic stem cell
20	chr1:210606800-210608200	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:210606800-210608200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:210606800-210608400	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr1:210607000-210607400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr1:210607000-210608200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr1:210607200-210608000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr1:210607200-210608200	Enhancers	HSMMtube	muscle
27	chr1:210607400-210607600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr1:210607400-210608200	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr1:210607600-210608000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr1:210607600-210608200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr1:210607600-210608200	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr1:210608000-210608400	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr1:210608000-210612000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
34	chr1:210608000-210612200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr1:210608200-210609800	Weak transcription	HSMMtube	muscle
36	chr1:210608200-210612200	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr1:210608200-210612200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr1:210608200-210612800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr1:210608400-210608800	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
40	chr1:210608800-210610200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr1:210609200-210619800	Weak transcription	Esophagus	oesophagus
42	chr1:210609800-210612800	Enhancers	HSMMtube	muscle
43	chr1:210610000-210610600	Genic enhancers	HSMM	muscle
44	chr1:210610200-210613800	Enhancers	Muscle Satellite Cultured Cells	--
45	chr1:210610600-210612400	Enhancers	HSMM	muscle
46	chr1:210610600-210612800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
47	chr1:210610600-210613000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
48	chr1:210610600-210614800	Enhancers	Fetal Muscle Leg	muscle
49	chr1:210610600-210615000	Enhancers	Osteobl	bone
50	chr1:210610800-210611600	Strong transcription	Aorta	Aorta

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