Variant report

Variant	nsv885949
Chromosome Location	chr6:57720549-58144557
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:415)
CpG islands
(count:611)
Chromatin interactive
region (count:1)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:415 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:57996881-57996935	K562	blood:	n/a	n/a
2	ATF3	chr6:58142478-58142721	A549	lung:	n/a	n/a
3	ATF3	chr6:58141691-58142004	K562	blood:	n/a	n/a
4	ATF3	chr6:58142472-58142715	K562	blood:	n/a	n/a
5	CEBPB	chr6:57813381-57813566	IMR90	lung:	n/a	chr6:57813503-57813514
6	CEBPB	chr6:57837290-57837331	A549	lung:	n/a	n/a
7	CEBPB	chr6:57813456-57813566	A549	lung:	n/a	chr6:57813503-57813514
8	CEBPB	chr6:57813363-57813589	HepG2	liver:	n/a	chr6:57813503-57813514
9	CEBPB	chr6:57835893-57836113	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:58030489-58030521	HepG2	liver:	n/a	chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499 chr6:58030490-58030499 chr6:58030490-58030501 chr6:58030490-58030499
11	CEBPB	chr6:57837128-57837338	HepG2	liver:	n/a	chr6:57837142-57837155
12	CHD2	chr6:57757439-57757666	K562	blood:	n/a	n/a
13	CTCF	chr6:57778614-57778670	MCF-7	breast:	n/a	n/a
14	CTCF	chr6:57903824-57904064	K562	blood:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
15	CTCF	chr6:57811449-57811640	MCF-7	breast:	n/a	n/a
16	CTCF	chr6:57722820-57722876	GM19239	blood:	n/a	n/a
17	CTCF	chr6:57754514-57754622	HepG2	liver:	n/a	n/a
18	CTCF	chr6:57766986-57767109	Hela-S3	cervix:	n/a	n/a
19	CTCF	chr6:57869798-57869852	GM20000	blood:	n/a	n/a
20	CTCF	chr6:57722720-57722870	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr6:57740614-57740646	GM10248	blood:	n/a	n/a
22	CTCF	chr6:57766851-57767168	LNCaP	prostate:	n/a	n/a
23	CTCF	chr6:57798424-57798467	LNCaP	prostate:	n/a	n/a
24	CTCF	chr6:57766980-57767130	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr6:57832685-57832716	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr6:57722752-57722918	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:57722760-57722910	HMEC	breast:	n/a	n/a
28	CTCF	chr6:57811483-57811592	ProgFib	skin:	n/a	n/a
29	CTCF	chr6:57767018-57767160	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:57811430-57811659	MCF-7	breast:	n/a	n/a
31	CTCF	chr6:57903580-57903730	HEEpiC	esophagus:	n/a	n/a
32	CTCF	chr6:57811480-57811630	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr6:57811220-57811370	NHEK	skin:	n/a	n/a
34	CTCF	chr6:57767034-57767099	Lung_OC	lung:	n/a	n/a
35	CTCF	chr6:57722755-57722897	K562	blood:	n/a	n/a
36	CTCF	chr6:57726550-57726650	LNCaP	prostate:	n/a	n/a
37	CTCF	chr6:58025840-58025911	Medullo	brain:	n/a	n/a
38	CTCF	chr6:57767018-57767174	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:57903946-57903972	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:57732417-57732486	Lung_OC	lung:	n/a	n/a
41	CTCF	chr6:57903680-57903830	HMF	breast:	n/a	n/a
42	CTCF	chr6:57767040-57767190	MCF-7	breast:	n/a	n/a
43	CTCF	chr6:57811420-57811570	NHEK	skin:	n/a	chr6:57811427-57811440
44	CTCF	chr6:57767031-57767102	ProgFib	skin:	n/a	n/a
45	CTCF	chr6:57811450-57811652	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:57903855-57904044	Spleen_OC	spleen:	n/a	chr6:57903906-57903927 chr6:57903911-57903929
47	CTCF	chr6:57811466-57811623	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr6:57722787-57722907	LNCaP	prostate:	n/a	n/a
49	CTCF	chr6:57725922-57726015	ProgFib	skin:	n/a	n/a
50	CTCF	chr6:57976615-57976701	GM13977	blood:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:58141890-58141940	GM06990	blood:	n/a
2	chr6:58141890-58141940	GM06990	blood:	n/a
3	chr6:57972680-57972730	HEK293	kidney:	embryo
4	chr6:58001971-58002021	PrEC	prostate:	n/a
5	chr6:58141890-58141940	AoSMC	blood vessel:	n/a
6	chr6:57972349-57972399	HNPCEpiC	eye:	n/a
7	chr6:57972349-57972399	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:57970592-57970642	GM12891	blood:	n/a
9	chr6:57970666-57970716	U87	brain:	n/a
10	chr6:57972721-57972771	CMK	blood:	n/a
11	chr6:58001971-58002021	Hela-S3	cervix:	n/a
12	chr6:57912662-57912712	HIPEpiC	eye:	n/a
13	chr6:57972680-57972730	HAEpiC	amniotic membrane:	n/a
14	chr6:57972680-57972730	MCF-7	breast:	n/a
15	chr6:57970666-57970716	HCF	heart:	n/a
16	chr6:57972680-57972730	PrEC	prostate:	n/a
17	chr6:57972223-57972273	LNCaP	prostate:	n/a
18	chr6:57972680-57972730	Hela-S3	cervix:	n/a
19	chr6:58141890-58141940	NHDF-neo	bronchial:	n/a
20	chr6:57912662-57912712	HCPEpiC	choroid plexus:	n/a
21	chr6:57972680-57972730	ECC-1	luminal epithelium:	n/a
22	chr6:57972223-57972273	T-47D	breast:	n/a
23	chr6:57970592-57970642	HCPEpiC	choroid plexus:	n/a
24	chr6:57912662-57912712	MCF-7	breast:	n/a
25	chr6:57972349-57972399	HepG2	liver:	n/a
26	chr6:57972680-57972730	K562	blood:	n/a
27	chr6:57972223-57972273	GM12891	blood:	n/a
28	chr6:57970666-57970716	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:58001971-58002021	HepG2	liver:	n/a
30	chr6:57972223-57972273	HAEpiC	amniotic membrane:	n/a
31	chr6:57970592-57970642	HCM	heart:	n/a
32	chr6:58142044-58142094	NT2-D1	testis:	n/a
33	chr6:57972721-57972771	SK-N-SH	brain:	n/a
34	chr6:58142044-58142094	AG09319	gingival:	n/a
35	chr6:57972223-57972273	NT2-D1	testis:	n/a
36	chr6:58001971-58002021	RPTEC	kidney:	n/a
37	chr6:57970592-57970642	SKMC	muscle:	n/a
38	chr6:57970592-57970642	RPTEC	kidney:	n/a
39	chr6:57972680-57972730	AG09319	gingival:	n/a
40	chr6:57972349-57972399	MCF-7	breast:	n/a
41	chr6:57970592-57970642	HRE	kidney:	n/a
42	chr6:57972721-57972771	H1-hESC	embryonic stem cell:	embryo
43	chr6:58001971-58002021	ECC-1	luminal epithelium:	n/a
44	chr6:57972223-57972273	HRPEpiC	eye:	n/a
45	chr6:57972721-57972771	HPAEpiC	pulmonary alveolar:	n/a
46	chr6:57970592-57970642	NHDF-neo	bronchial:	n/a
47	chr6:57972680-57972730	HEEpiC	esophagus:	n/a
48	chr6:57912662-57912712	NHDF-neo	bronchial:	n/a
49	chr6:57972349-57972399	SK-N-MC	brain:	n/a
50	chr6:57972721-57972771	GM06990	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:57766644..57767228-chr6:62859661..62860581,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAB23-15	chr6:57793932-57794280	NONHSAT113301
2	lnc-BAG2-11	chr6:57798854-57798915	NONHSAT113302
3	lnc-BAG2-11	chr6:57799352-57799604	NONHSAT113302

No data

Variant related genes	Relation type
ENSG00000270213	TF binding region
ENSG00000262828	TF binding region
RBBP4P3	TF binding region
ENSG00000270213	CpG island
ENSG00000262828	CpG island
RBBP4P3	CpG island

Extended variants
information (count: 2066 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2066 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs373673767	chr6:57726403-57726404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192738499	chr6:57726408-57726409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs541396423	chr6:57726471-57726472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376148873	chr6:57726473-57726474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs201795613	chr6:57726476-57726477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs4458690	chr6:57726477-57726478	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs61095852	chr6:57726500-57726501	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371061761	chr6:57726532-57726533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530754222	chr6:57726611-57726612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs552443646	chr6:57726623-57726624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs564130725	chr6:57726631-57726632	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556164622	chr6:57726668-57726669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576384202	chr6:57726713-57726714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs528255998	chr6:57726729-57726730	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs547134186	chr6:57726757-57726758	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs539091702	chr6:57726758-57726759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548133073	chr6:57726766-57726767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs182109455	chr6:57726850-57726851	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs550736100	chr6:57726913-57726914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs187226633	chr6:57726917-57726918	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs550775909	chr6:57726935-57726936	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs539788283	chr6:57726955-57726956	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs191713799	chr6:57726987-57726988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184629758	chr6:57727044-57727045	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs534091193	chr6:57727087-57727088	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9396416	chr6:57727093-57727094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs574220460	chr6:57727099-57727100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs189057408	chr6:57727139-57727140	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs376296069	chr6:57727148-57727149	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs563184338	chr6:57727203-57727204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs575130523	chr6:57727224-57727225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550151019	chr6:57727251-57727252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374607753	chr6:57727283-57727284	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141631373	chr6:57727333-57727334	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs6938380	chr6:57727343-57727344	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs546846281	chr6:57727405-57727406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561852929	chr6:57727437-57727438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs193140955	chr6:57727475-57727476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs551048472	chr6:57727493-57727494	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs11753022	chr6:57727505-57727506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs569158784	chr6:57727556-57727557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533315434	chr6:57727558-57727559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs551801615	chr6:57727621-57727622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs566795012	chr6:57727628-57727629	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs150436230	chr6:57727690-57727691	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs116575647	chr6:57727693-57727694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs567518349	chr6:57727707-57727708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs185718838	chr6:57727726-57727727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs28589486	chr6:57727742-57727743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556977923	chr6:57727754-57727755	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	CNVD
Neuroblastoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	17603634	CNVD
Systemic lupus erythematosus	17503323	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	16608533	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD

Chromatin state (count:181 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:57726400-57726600	Enhancers	Fetal Intestine Small	intestine
2	chr6:57726600-57727200	Weak transcription	Fetal Intestine Small	intestine
3	chr6:57726600-57727800	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr6:57727200-57727800	Enhancers	Fetal Intestine Small	intestine
5	chr6:57727400-57727800	Enhancers	Fetal Intestine Large	intestine
6	chr6:57727400-57728000	Enhancers	Rectal Mucosa Donor 29	rectum
7	chr6:57727600-57729600	Enhancers	Dnd41	blood
8	chr6:57734800-57736800	Enhancers	Fetal Intestine Large	intestine
9	chr6:57735000-57736800	Enhancers	Fetal Intestine Small	intestine
10	chr6:57746800-57747800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr6:57747400-57748000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:57748000-57748400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr6:57748400-57748800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr6:57749800-57750000	Enhancers	Fetal Intestine Large	intestine
15	chr6:57750000-57751200	Weak transcription	Fetal Intestine Large	intestine
16	chr6:57750200-57751800	Enhancers	Fetal Intestine Small	intestine
17	chr6:57751200-57751800	Enhancers	Fetal Intestine Large	intestine
18	chr6:57760200-57760600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr6:57766400-57766800	Enhancers	Brain Cingulate Gyrus	brain
20	chr6:57766400-57766800	Enhancers	Brain Hippocampus Middle	brain
21	chr6:57766600-57767000	Enhancers	Fetal Brain Male	brain
22	chr6:57766800-57767000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr6:57766800-57767200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
24	chr6:57767400-57768400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr6:57768400-57768800	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr6:57768400-57769200	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr6:57768400-57769200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr6:57789800-57790400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr6:57790000-57790600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr6:57808400-57808800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr6:57808800-57810400	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr6:57810400-57812000	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr6:57810400-57812000	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr6:57810600-57811400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr6:57810600-57812000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:57810600-57812000	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr6:57811200-57812000	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr6:57832800-57833600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr6:57833600-57838600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:57835000-57835400	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr6:57835000-57835600	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:57835000-57835600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr6:57835000-57835600	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:57835000-57836000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr6:57835400-57836000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr6:57835400-57849000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
47	chr6:57835600-57838800	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr6:57835600-57838800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
49	chr6:57836000-57838800	Weak transcription	HUES64 Cell Line	embryonic stem cell
50	chr6:57838600-57839400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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