Variant report

Variant	esv3346394
Chromosome Location	chr14:21183732-21194448
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:32)
CpG islands
(count:305)
Chromatin interactive
region (count:5)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:32 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr14:21188058-21188376	GM12878	blood:	n/a	n/a
2	CEBPB	chr14:21189120-21189266	A549	lung:	n/a	chr14:21189167-21189178
3	CEBPB	chr14:21189109-21189267	IMR90	lung:	n/a	chr14:21189167-21189178
4	CEBPB	chr14:21189093-21189216	HepG2	liver:	n/a	chr14:21189167-21189178
5	CEBPB	chr14:21184306-21184396	K562	blood:	n/a	n/a
6	CEBPB	chr14:21189089-21189189	K562	blood:	n/a	chr14:21189167-21189178
7	CTCF	chr14:21191665-21191916	H1-hESC	embryonic stem cell:	n/a	chr14:21191792-21191805
8	CTCF	chr14:21191748-21191869	H1-hESC	embryonic stem cell:	n/a	chr14:21191792-21191805
9	CTCF	chr14:21184520-21184670	GM12873	blood:	n/a	n/a
10	CTCF	chr14:21184597-21184618	HepG2	liver:	n/a	n/a
11	CTCF	chr14:21184500-21184650	HEK293	kidney:	n/a	n/a
12	E2F6	chr14:21191696-21191863	K562	blood:	n/a	chr14:21191788-21191798 chr14:21191782-21191792 chr14:21191785-21191795
13	E2F6	chr14:21191663-21191960	H1-hESC	embryonic stem cell:	n/a	chr14:21191788-21191798 chr14:21191782-21191792 chr14:21191785-21191795
14	GATA3	chr14:21187797-21188427	MCF-7	breast:	n/a	n/a
15	GATA3	chr14:21187628-21188560	MCF-7	breast:	n/a	n/a
16	MAFK	chr14:21190555-21190630	HepG2	liver:	n/a	chr14:21190586-21190606
17	MAFK	chr14:21190573-21190717	HepG2	liver:	n/a	chr14:21190586-21190606
18	MAX	chr14:21191597-21191910	H1-hESC	embryonic stem cell:	n/a	chr14:21191654-21191664
19	MAX	chr14:21191691-21191940	H1-hESC	embryonic stem cell:	n/a	n/a
20	PAX5	chr14:21187981-21188224	GM12878	blood:	n/a	n/a
21	POLR2A	chr14:21191242-21191339	GM12878	blood:	n/a	n/a
22	POLR2A	chr14:21190985-21191067	GM12878	blood:	n/a	n/a
23	RAD21	chr14:21191529-21192013	H1-hESC	embryonic stem cell:	n/a	n/a
24	RCOR1	chr14:21191865-21191868	K562	blood:	n/a	n/a
25	RUNX3	chr14:21187826-21188211	GM12878	blood:	n/a	n/a
26	RUNX3	chr14:21187811-21188240	GM12878	blood:	n/a	n/a
27	SPI1	chr14:21183630-21183869	GM12878	blood:	n/a	n/a
28	SPI1	chr14:21183688-21183913	HL-60	blood:	n/a	n/a
29	TCF7L2	chr14:21187979-21188251	MCF-7	breast:	n/a	n/a
30	UBTF	chr14:21191673-21191706	K562	blood:	n/a	n/a
31	ZNF217	chr14:21187990-21188319	MCF-7	breast:	n/a	n/a
32	ZNF384	chr14:21183795-21183860	GM12878	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21191859-21191909	SK-N-SH_RA	brain:	n/a
2	chr14:21193994-21194044	NT2-D1	testis:	n/a
3	chr14:21190377-21190427	HL-60	blood:	n/a
4	chr14:21192743-21192793	HRPEpiC	eye:	n/a
5	chr14:21192743-21192793	MCF-7	breast:	n/a
6	chr14:21192743-21192793	SK-N-SH	brain:	n/a
7	chr14:21191754-21191804	ovcar-3	ovarian:	n/a
8	chr14:21190377-21190427	PANC-1	pancreas:	n/a
9	chr14:21192743-21192793	Caco-2	colon:	n/a
10	chr14:21193994-21194044	ovcar-3	ovarian:	n/a
11	chr14:21191859-21191909	AG09319	gingival:	n/a
12	chr14:21191859-21191909	HNPCEpiC	eye:	n/a
13	chr14:21191859-21191909	HL-60	blood:	n/a
14	chr14:21190377-21190427	BE2_C	brain:	n/a
15	chr14:21191859-21191909	RPTEC	kidney:	n/a
16	chr14:21191754-21191804	AG04449	skin:	fetal
17	chr14:21192743-21192793	ovcar-3	ovarian:	n/a
18	chr14:21191754-21191804	HCF	heart:	n/a
19	chr14:21191859-21191909	HCPEpiC	choroid plexus:	n/a
20	chr14:21192743-21192793	HMEC	breast:	n/a
21	chr14:21193994-21194044	NB4	blood:	n/a
22	chr14:21192743-21192793	HEEpiC	esophagus:	n/a
23	chr14:21192743-21192793	HIPEpiC	eye:	n/a
24	chr14:21190377-21190427	AG04450	lung:	fetal
25	chr14:21191859-21191909	PANC-1	pancreas:	n/a
26	chr14:21192743-21192793	PFSK-1	brain:	n/a
27	chr14:21191754-21191804	SKMC	muscle:	n/a
28	chr14:21192743-21192793	HEK293	kidney:	embryo
29	chr14:21191859-21191909	AoSMC	blood vessel:	n/a
30	chr14:21190377-21190427	PFSK-1	brain:	n/a
31	chr14:21193994-21194044	HIPEpiC	eye:	n/a
32	chr14:21191859-21191909	MCF10A-Er-Src	breast:	n/a
33	chr14:21191859-21191909	SK-N-MC	brain:	n/a
34	chr14:21191859-21191909	ProgFib	skin:	n/a
35	chr14:21193994-21194044	HEEpiC	esophagus:	n/a
36	chr14:21191859-21191909	GM12891	blood:	n/a
37	chr14:21192743-21192793	AG09319	gingival:	n/a
38	chr14:21191754-21191804	SK-N-SH_RA	brain:	n/a
39	chr14:21192743-21192793	HRCEpiC	kidney:	n/a
40	chr14:21193994-21194044	MCF10A-Er-Src	breast:	n/a
41	chr14:21191754-21191804	NHDF-neo	bronchial:	n/a
42	chr14:21192743-21192793	CMK	blood:	n/a
43	chr14:21191754-21191804	AG10803	skin:	n/a
44	chr14:21191859-21191909	HRE	kidney:	n/a
45	chr14:21191859-21191909	K562	blood:	n/a
46	chr14:21193994-21194044	T-47D	breast:	n/a
47	chr14:21191754-21191804	HMEC	breast:	n/a
48	chr14:21190377-21190427	NT2-D1	testis:	n/a
49	chr14:21190377-21190427	Jurkat	blood:	n/a
50	chr14:21190377-21190427	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:21180210..21181915-chr14:21183845..21185630,2	MCF-7	breast:
2	chr14:21192360..21195343-chr14:21197458..21200150,2	MCF-7	breast:
3	chr14:21187061..21189567-chr14:21198375..21200452,2	K562	blood:
4	chr14:21173697..21176049-chr14:21188809..21190635,2	MCF-7	breast:
5	chr14:21173340..21178331-chr14:21181537..21185629,5	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EDDM3A-1	chr14:21189355-21190638	NONHSAT035608

No data

Variant related genes	Relation type
RANBP20P	TF binding region
RANBP20P	CpG island
ENSG00000258451	chromatin interactions

Extended variants
information (count: 505 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:505 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531295376	chr14:21183733-21183734	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549777405	chr14:21183744-21183745	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs561514606	chr14:21183799-21183800	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs528848814	chr14:21183800-21183801	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs548923518	chr14:21183803-21183804	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139766222	chr14:21183806-21183807	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs534402667	chr14:21183832-21183833	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs149972473	chr14:21183836-21183837	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570973026	chr14:21183844-21183845	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs367598941	chr14:21183866-21183867	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs75115486	chr14:21183881-21183882	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs193182810	chr14:21183889-21183890	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs556554046	chr14:21183905-21183906	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs568376806	chr14:21183949-21183950	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs535430260	chr14:21183957-21183958	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557211484	chr14:21183984-21183985	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576113203	chr14:21184012-21184013	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs61447943	chr14:21184023-21184024	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs185112520	chr14:21184058-21184059	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs564913404	chr14:21184081-21184082	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs149163831	chr14:21184086-21184087	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs8010445	chr14:21184167-21184168	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs543171827	chr14:21184183-21184184	Enhancers Weak transcription Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs190801161	chr14:21184208-21184209	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs116778926	chr14:21184259-21184260	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs192525576	chr14:21184277-21184278	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs559609133	chr14:21184295-21184296	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs529816083	chr14:21184349-21184350	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184750504	chr14:21184364-21184365	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376417965	chr14:21184386-21184387	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs114848411	chr14:21184392-21184393	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs527988876	chr14:21184395-21184396	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs528368273	chr14:21184396-21184397	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs570939979	chr14:21184445-21184446	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs74993266	chr14:21184467-21184468	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs8015364	chr14:21184482-21184483	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs568492426	chr14:21184486-21184487	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs114178563	chr14:21184522-21184523	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs553738856	chr14:21184552-21184553	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114426582	chr14:21184575-21184576	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs539333478	chr14:21184576-21184577	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs147820027	chr14:21184577-21184578	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs576181681	chr14:21184578-21184579	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs188347383	chr14:21184594-21184595	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555180274	chr14:21184598-21184599	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs552145307	chr14:21184614-21184615	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs180759670	chr14:21184625-21184626	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs76672847	chr14:21184629-21184630	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs146989628	chr14:21184646-21184647	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs540360449	chr14:21184648-21184649	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Breast cancer	21364760	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
small cell lung cancer	17426248	CNVD

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21168000-21194600	Weak transcription	Gastric	stomach
2	chr14:21176400-21187600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr14:21178800-21183800	Enhancers	Stomach Mucosa	stomach
4	chr14:21180000-21184200	Enhancers	Primary B cells from cord blood	blood
5	chr14:21182200-21185600	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr14:21182800-21183800	Enhancers	Brain Substantia Nigra	brain
7	chr14:21183000-21185800	Enhancers	Primary B cells from peripheral blood	blood
8	chr14:21183200-21184200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
9	chr14:21183200-21187600	Weak transcription	Duodenum Mucosa	Duodenum
10	chr14:21183400-21183800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr14:21183400-21187600	Weak transcription	Pancreas	Pancrea
12	chr14:21183600-21183800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr14:21183600-21184200	Active TSS	Monocytes-CD14+_RO01746	blood
14	chr14:21183600-21185400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr14:21183800-21186600	Weak transcription	Stomach Mucosa	stomach
16	chr14:21184200-21184600	Flanking Active TSS	Primary B cells from cord blood	blood
17	chr14:21184200-21184800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
18	chr14:21184400-21184600	Enhancers	Esophagus	oesophagus
19	chr14:21184600-21188600	Enhancers	Primary B cells from cord blood	blood
20	chr14:21184800-21185600	Enhancers	Monocytes-CD14+_RO01746	blood
21	chr14:21185600-21187000	Weak transcription	Rectal Mucosa Donor 29	rectum
22	chr14:21185800-21187600	Weak transcription	Primary B cells from peripheral blood	blood
23	chr14:21186600-21188600	Enhancers	Fetal Intestine Small	intestine
24	chr14:21186600-21189200	Enhancers	Fetal Intestine Large	intestine
25	chr14:21186600-21189200	Enhancers	Stomach Mucosa	stomach
26	chr14:21186800-21188400	Enhancers	Sigmoid Colon	Sigmoid Colon
27	chr14:21186800-21189200	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr14:21187000-21187600	Enhancers	Rectal Mucosa Donor 29	rectum
29	chr14:21187400-21188600	Enhancers	Placenta Amnion	Placenta Amnion
30	chr14:21187600-21187800	Enhancers	Fetal Thymus	thymus
31	chr14:21187600-21188000	Flanking Active TSS	Rectal Mucosa Donor 29	rectum
32	chr14:21187600-21188200	Enhancers	Primary B cells from peripheral blood	blood
33	chr14:21187600-21188200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr14:21187600-21188600	Enhancers	Duodenum Mucosa	Duodenum
35	chr14:21187600-21189200	Enhancers	Pancreas	Pancrea
36	chr14:21187800-21188200	Enhancers	GM12878-XiMat	blood
37	chr14:21187800-21198800	Weak transcription	Fetal Heart	heart
38	chr14:21188000-21188600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr14:21188000-21188800	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr14:21188200-21191200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr14:21188400-21189000	Enhancers	Fetal Kidney	kidney
42	chr14:21188600-21191200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr14:21189000-21189200	Enhancers	Fetal Lung	lung
44	chr14:21189200-21190600	Weak transcription	Pancreas	Pancrea
45	chr14:21189200-21194600	Weak transcription	Stomach Mucosa	stomach
46	chr14:21189600-21201600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:21190600-21190800	Enhancers	Pancreas	Pancrea
48	chr14:21191200-21191400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:21191200-21191400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr14:21191200-21191400	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood

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