Variant report

Variant	nsv1045788
Chromosome Location	chr14:24455413-24489426
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:774)
CpG islands
(count:1099)
Chromatin interactive
region (count:9)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:774 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24483175-24483522	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:24483172-24483507	K562	blood:	n/a	n/a
3	ATF2	chr14:24458816-24459305	GM12878	blood:	n/a	n/a
4	BACH1	chr14:24476252-24476312	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr14:24458105-24458174	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr14:24458905-24459223	GM12878	blood:	n/a	n/a
7	BATF	chr14:24458871-24459266	GM12878	blood:	n/a	n/a
8	BHLHE40	chr14:24483187-24483465	GM12878	blood:	n/a	n/a
9	BHLHE40	chr14:24456162-24456216	HepG2	liver:	n/a	n/a
10	BHLHE40	chr14:24483227-24483438	K562	blood:	n/a	n/a
11	BHLHE40	chr14:24475943-24476541	HepG2	liver:	n/a	n/a
12	BRCA1	chr14:24483351-24483423	GM12878	blood:	n/a	n/a
13	CBX3	chr14:24483227-24483553	K562	blood:	n/a	n/a
14	CBX3	chr14:24483218-24483539	K562	blood:	n/a	n/a
15	CBX3	chr14:24476155-24476416	K562	blood:	n/a	n/a
16	CEBPB	chr14:24456316-24456341	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:24482978-24483461	A549	lung:	n/a	n/a
18	CEBPD	chr14:24455859-24456293	HepG2	liver:	n/a	n/a
19	CEBPD	chr14:24457835-24458170	HepG2	liver:	n/a	n/a
20	CEBPD	chr14:24457723-24458280	HepG2	liver:	n/a	n/a
21	CEBPD	chr14:24475992-24476248	HepG2	liver:	n/a	n/a
22	CHD1	chr14:24483316-24483498	GM12878	blood:	n/a	n/a
23	CHD2	chr14:24457926-24458005	Hela-S3	cervix:	n/a	chr14:24457984-24457994
24	CHD2	chr14:24483281-24483447	GM12878	blood:	n/a	n/a
25	CTCF	chr14:24483205-24483492	A549	lung:	n/a	n/a
26	CTCF	chr14:24489280-24489430	HRPEpiC	eye:	n/a	n/a
27	CTCF	chr14:24483280-24483430	GM06990	blood:	n/a	n/a
28	CTCF	chr14:24483333-24483377	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr14:24483280-24483430	GM12872	blood:	n/a	n/a
30	CTCF	chr14:24483260-24483410	AoAF	blood vessel:	n/a	n/a
31	CTCF	chr14:24489360-24489510	HMEC	breast:	n/a	n/a
32	CTCF	chr14:24489380-24489530	HAc	cerebellar:	n/a	n/a
33	CTCF	chr14:24489360-24489510	SAEC	small airway:	n/a	n/a
34	CTCF	chr14:24483129-24483607	HCT-116	colon:	n/a	n/a
35	CTCF	chr14:24489340-24489490	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr14:24483220-24483370	HCM	heart:	n/a	n/a
37	CTCF	chr14:24483201-24483483	GM12878	blood:	n/a	n/a
38	CTCF	chr14:24483240-24483390	HRPEpiC	eye:	n/a	n/a
39	CTCF	chr14:24489260-24489410	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr14:24489338-24489458	GM20000	blood:	n/a	n/a
41	CTCF	chr14:24489400-24489550	BE2_C	brain:	n/a	n/a
42	CTCF	chr14:24489340-24489490	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr14:24483200-24483477	HepG2	liver:	n/a	n/a
44	CTCF	chr14:24483242-24483413	GM20000	blood:	n/a	n/a
45	CTCF	chr14:24489280-24489430	AG10803	skin:	n/a	n/a
46	CTCF	chr14:24483309-24483422	GM12891	blood:	n/a	n/a
47	CTCF	chr14:24458502-24458607	GM19238	blood:	n/a	n/a
48	CTCF	chr14:24489340-24489490	NHDF-neo	bronchial:	n/a	n/a
49	CTCF	chr14:24483240-24483390	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr14:24489360-24489510	HPF	lung:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24476478-24476528	HCT-116	colon:	n/a
2	chr14:24476478-24476528	HCT-116	colon:	n/a
3	chr14:24475906-24475956	Hela-S3	cervix:	n/a
4	chr14:24476082-24476132	T-47D	breast:	n/a
5	chr14:24458004-24458054	GM12891	blood:	n/a
6	chr14:24476559-24476609	BJ	skin:	n/a
7	chr14:24458208-24458258	NHDF-neo	bronchial:	n/a
8	chr14:24458099-24458149	T-47D	breast:	n/a
9	chr14:24475053-24475103	ovcar-3	ovarian:	n/a
10	chr14:24457893-24457943	GM19239	blood:	n/a
11	chr14:24476082-24476132	Jurkat	blood:	n/a
12	chr14:24457509-24457559	HAEpiC	amniotic membrane:	n/a
13	chr14:24458345-24458395	NB4	blood:	n/a
14	chr14:24457893-24457943	SK-N-SH	brain:	n/a
15	chr14:24476559-24476609	NHDF-neo	bronchial:	n/a
16	chr14:24458208-24458258	A549	lung:	n/a
17	chr14:24458345-24458395	SK-N-MC	brain:	n/a
18	chr14:24457915-24457965	HRCEpiC	kidney:	n/a
19	chr14:24473832-24473882	ECC-1	luminal epithelium:	n/a
20	chr14:24457509-24457559	NH-A	brain:	n/a
21	chr14:24458208-24458258	HL-60	blood:	n/a
22	chr14:24475906-24475956	GM12891	blood:	n/a
23	chr14:24475053-24475103	Hela-S3	cervix:	n/a
24	chr14:24476559-24476609	Hepatocyte	liver:	n/a
25	chr14:24457915-24457965	HAEpiC	amniotic membrane:	n/a
26	chr14:24458208-24458258	HEEpiC	esophagus:	n/a
27	chr14:24457915-24457965	AG09309	skin:	n/a
28	chr14:24458000-24458050	Hela-S3	cervix:	n/a
29	chr14:24476478-24476528	PFSK-1	brain:	n/a
30	chr14:24478620-24478670	HMEC	breast:	n/a
31	chr14:24473832-24473882	HRPEpiC	eye:	n/a
32	chr14:24457893-24457943	Hela-S3	cervix:	n/a
33	chr14:24476478-24476528	HCM	heart:	n/a
34	chr14:24475053-24475103	GM12892	blood:	n/a
35	chr14:24458208-24458258	K562	blood:	n/a
36	chr14:24458345-24458395	NT2-D1	testis:	n/a
37	chr14:24458014-24458064	AG10803	skin:	n/a
38	chr14:24475053-24475103	SK-N-SH	brain:	n/a
39	chr14:24458299-24458349	MCF-7	breast:	n/a
40	chr14:24473832-24473882	ProgFib	skin:	n/a
41	chr14:24475053-24475103	PrEC	prostate:	n/a
42	chr14:24476478-24476528	K562	blood:	n/a
43	chr14:24478620-24478670	AG09319	gingival:	n/a
44	chr14:24457993-24458043	SKMC	muscle:	n/a
45	chr14:24458000-24458050	BJ	skin:	n/a
46	chr14:24476559-24476609	GM12891	blood:	n/a
47	chr14:24476478-24476528	HNPCEpiC	eye:	n/a
48	chr14:24457893-24457943	HCM	heart:	n/a
49	chr14:24458014-24458064	GM12892	blood:	n/a
50	chr14:24458345-24458395	HEEpiC	esophagus:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:24483262..24483795-chr14:24906005..24906586,2	K562	blood:
2	chr14:24482840..24483718-chr14:24710880..24711620,2	MCF-7	breast:
3	chr14:24476695..24479385-chr14:24563251..24564763,2	MCF-7	breast:
4	chr14:24482659..24484974-chr14:24503307..24504865,2	MCF-7	breast:
5	chr14:24482802..24483800-chr14:24505642..24506553,4	MCF-7	breast:
6	chr14:24483165..24483827-chr14:24559565..24560642,4	MCF-7	breast:
7	chr14:24421533..24423333-chr14:24480435..24482151,2	K562	blood:
8	chr14:24482946..24483934-chr14:24503845..24504435,3	MCF-7	breast:
9	chr14:24482858..24483785-chr14:24559502..24560237,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-1	chr14:24457938-24458048	ENSG00000215256.3

No data

Variant related genes	Relation type
DHRS4L2	TF binding region
DHRS4-AS1	TF binding region
DHRS4L2	CpG island
DHRS4-AS1	CpG island
ENSG00000215256	chromatin interactions
ENSG00000092330	chromatin interactions
ENSG00000225766	chromatin interactions
ENSG00000100889	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000129535	chromatin interactions

Extended variants
information (count: 1739 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:1739 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548530617	chr14:24455414-24455415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs189962995	chr14:24455415-24455416	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111808647	chr14:24455429-24455430	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574227681	chr14:24455431-24455432	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs12161886	chr14:24455456-24455457	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs374104063	chr14:24455499-24455500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs577456727	chr14:24455502-24455503	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs540032390	chr14:24455504-24455505	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs539747387	chr14:24455536-24455537	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs372640401	chr14:24455537-24455538	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148843815	chr14:24455552-24455553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs118079848	chr14:24455569-24455570	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs202202793	chr14:24455631-24455632	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547471380	chr14:24455633-24455634	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112907500	chr14:24455647-24455648	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs74828551	chr14:24455648-24455649	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs541080687	chr14:24455682-24455683	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs180804463	chr14:24455698-24455699	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs532891727	chr14:24455717-24455718	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs57039977	chr14:24455725-24455726	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs111339969	chr14:24455726-24455727	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs200315151	chr14:24455728-24455729	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs202088341	chr14:24455730-24455731	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs57989528	chr14:24455738-24455739	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs57215727	chr14:24455742-24455743	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs367578545	chr14:24455755-24455756	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs548479757	chr14:24455759-24455760	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs529122221	chr14:24455762-24455763	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs549008608	chr14:24455766-24455767	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs568400023	chr14:24455789-24455790	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs533929026	chr14:24455791-24455792	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs547813620	chr14:24455802-24455803	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs570938833	chr14:24455803-24455804	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs140806612	chr14:24455885-24455886	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs186490724	chr14:24455897-24455898	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs371521984	chr14:24455908-24455909	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs576733564	chr14:24455909-24455910	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs536101191	chr14:24455912-24455913	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs555796550	chr14:24455917-24455918	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs572739583	chr14:24455928-24455929	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs540667077	chr14:24455930-24455931	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs570356693	chr14:24455938-24455939	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs144630805	chr14:24455954-24455955	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs148164857	chr14:24455959-24455960	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs543134300	chr14:24455965-24455966	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs141347994	chr14:24455986-24455987	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs563095201	chr14:24455987-24455988	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs374911295	chr14:24455991-24455992	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs369310282	chr14:24455996-24455997	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs559381841	chr14:24456013-24456014	Enhancers Flanking Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
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
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
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Breast cancer	21364760	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Glioblastoma multiforme	21390271	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24424000-24458000	Weak transcription	Primary T cells from cord blood	blood
2	chr14:24439400-24457600	Weak transcription	Primary T helper cells fromperipheralblood	blood
3	chr14:24442800-24456000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr14:24445200-24456200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
5	chr14:24446200-24458000	Weak transcription	Gastric	stomach
6	chr14:24446600-24457400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr14:24448000-24457400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr14:24448400-24457400	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr14:24450400-24457400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr14:24450400-24457600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr14:24451800-24457400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
12	chr14:24452000-24455800	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr14:24452600-24457600	Weak transcription	Primary T helper cells PMA-I stimulated	--
14	chr14:24453600-24457600	Enhancers	Dnd41	blood
15	chr14:24453800-24456400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr14:24453800-24456400	Enhancers	Fetal Intestine Small	intestine
17	chr14:24453800-24457000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr14:24453800-24457000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr14:24453800-24457000	Enhancers	NHEK	skin
20	chr14:24453800-24457600	Enhancers	Fetal Thymus	thymus
21	chr14:24454000-24455800	Enhancers	HepG2	liver
22	chr14:24454000-24456000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr14:24454000-24456400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr14:24454200-24455800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr14:24454200-24456200	Enhancers	Psoas Muscle	Psoas
26	chr14:24454200-24456200	Enhancers	NHDF-Ad	bronchial
27	chr14:24454400-24455800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr14:24454600-24456000	Weak transcription	Adipose Nuclei	Adipose
29	chr14:24454600-24456200	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr14:24454600-24457000	Enhancers	Thymus	Thymus
31	chr14:24454800-24455800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr14:24454800-24455800	Weak transcription	Fetal Lung	lung
33	chr14:24454800-24455800	Weak transcription	Fetal Muscle Leg	muscle
34	chr14:24454800-24456000	Weak transcription	Duodenum Mucosa	Duodenum
35	chr14:24454800-24457600	Weak transcription	Skeletal Muscle Female	skeletal muscle
36	chr14:24455000-24456200	Enhancers	Placenta	Placenta
37	chr14:24455000-24456600	Enhancers	NHLF	lung
38	chr14:24455000-24457800	Weak transcription	HMEC	breast
39	chr14:24455000-24458000	Weak transcription	HSMM	muscle
40	chr14:24455200-24455600	Weak transcription	Rectal Mucosa Donor 29	rectum
41	chr14:24455200-24455600	Weak transcription	A549	lung
42	chr14:24455200-24456600	Enhancers	Esophagus	oesophagus
43	chr14:24455200-24457400	Weak transcription	Monocytes-CD14+_RO01746	blood
44	chr14:24455200-24457600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr14:24455200-24457600	Weak transcription	Osteobl	bone
46	chr14:24455400-24456200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:24455400-24456200	Enhancers	Sigmoid Colon	Sigmoid Colon
48	chr14:24455400-24457000	Weak transcription	Primary monocytes fromperipheralblood	blood
49	chr14:24455400-24457600	Enhancers	Fetal Intestine Large	intestine
50	chr14:24455400-24457800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links