Variant report

Variant	nsv901601
Chromosome Location	chr14:35101785-35131862
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:439)
CpG islands
(count:122)
Chromatin interactive
region (count:27)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:439 , 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	ARID3A	chr14:35108776-35108980	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35120180-35120293	K562	blood:	n/a	n/a
3	ARID3A	chr14:35110288-35110323	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35122450-35122628	K562	blood:	n/a	n/a
5	ATF1	chr14:35122319-35122681	K562	blood:	n/a	n/a
6	ATF3	chr14:35120025-35120546	A549	lung:	n/a	n/a
7	ATF3	chr14:35120100-35120458	K562	blood:	n/a	n/a
8	BCL3	chr14:35119887-35120614	A549	lung:	n/a	n/a
9	BHLHE40	chr14:35122438-35122531	K562	blood:	n/a	n/a
10	BHLHE40	chr14:35110689-35110801	K562	blood:	n/a	n/a
11	BRCA1	chr14:35103323-35103556	Hela-S3	cervix:	n/a	n/a
12	CBX3	chr14:35119917-35120633	HCT-116	colon:	n/a	n/a
13	CBX3	chr14:35119980-35120560	HCT-116	colon:	n/a	n/a
14	CBX3	chr14:35120163-35120474	K562	blood:	n/a	n/a
15	CCNT2	chr14:35125305-35125505	K562	blood:	n/a	n/a
16	CEBPB	chr14:35117883-35118178	K562	blood:	n/a	n/a
17	CEBPB	chr14:35117912-35118148	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr14:35117904-35118191	K562	blood:	n/a	n/a
19	CEBPB	chr14:35103532-35103836	K562	blood:	n/a	n/a
20	CEBPB	chr14:35119913-35120724	HCT-116	colon:	n/a	n/a
21	CEBPB	chr14:35120045-35120582	MCF-7	breast:	n/a	n/a
22	CEBPB	chr14:35117871-35118372	MCF-7	breast:	n/a	n/a
23	CEBPB	chr14:35119933-35120650	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr14:35119953-35120653	A549	lung:	n/a	n/a
25	CEBPB	chr14:35117932-35118134	HepG2	liver:	n/a	n/a
26	CEBPB	chr14:35117900-35118387	MCF-7	breast:	n/a	n/a
27	CEBPB	chr14:35119868-35120784	A549	lung:	n/a	n/a
28	CEBPB	chr14:35119880-35120558	A549	lung:	n/a	n/a
29	CEBPB	chr14:35119923-35120648	HCT-116	colon:	n/a	n/a
30	CEBPB	chr14:35119938-35120515	IMR90	lung:	n/a	n/a
31	CEBPB	chr14:35122373-35122856	K562	blood:	n/a	n/a
32	CEBPB	chr14:35103537-35103778	K562	blood:	n/a	n/a
33	CEBPB	chr14:35103470-35103768	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr14:35117951-35118138	A549	lung:	n/a	n/a
35	CEBPB	chr14:35117908-35118150	IMR90	lung:	n/a	n/a
36	CEBPB	chr14:35122283-35122841	K562	blood:	n/a	n/a
37	CEBPB	chr14:35120153-35120445	K562	blood:	n/a	n/a
38	CEBPD	chr14:35122197-35122711	K562	blood:	n/a	n/a
39	CEBPD	chr14:35122219-35122589	K562	blood:	n/a	n/a
40	CHD2	chr14:35108859-35108903	HepG2	liver:	n/a	n/a
41	CTCF	chr14:35108760-35108910	AoAF	blood vessel:	n/a	n/a
42	CTCF	chr14:35108960-35109110	WI-38	lung:	n/a	n/a
43	CTCF	chr14:35108760-35108910	HCM	heart:	n/a	n/a
44	CTCF	chr14:35108800-35108950	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr14:35108760-35108910	SAEC	small airway:	n/a	n/a
46	CTCF	chr14:35108795-35108903	MCF-7	breast:	n/a	n/a
47	CTCF	chr14:35108820-35108970	HEK293	kidney:	n/a	n/a
48	CTCF	chr14:35108740-35108890	A549	lung:	n/a	n/a
49	CTCF	chr14:35108780-35108930	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr14:35108860-35109010	WI-38	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35102433-35102483	Jurkat	blood:	n/a
2	chr14:35119021-35119071	HRCEpiC	kidney:	n/a
3	chr14:35119021-35119071	U87	brain:	n/a
4	chr14:35119021-35119071	HEEpiC	esophagus:	n/a
5	chr14:35102433-35102483	SAEC	small airway:	n/a
6	chr14:35102433-35102483	SKMC	muscle:	n/a
7	chr14:35102433-35102483	HCT-116	colon:	n/a
8	chr14:35102433-35102483	ECC-1	luminal epithelium:	n/a
9	chr14:35102433-35102483	BE2_C	brain:	n/a
10	chr14:35102433-35102483	HNPCEpiC	eye:	n/a
11	chr14:35102433-35102483	HCM	heart:	n/a
12	chr14:35119021-35119071	ProgFib	skin:	n/a
13	chr14:35119021-35119071	A549	lung:	n/a
14	chr14:35102433-35102483	HUVEC	blood vessel:	n/a
15	chr14:35119021-35119071	HCPEpiC	choroid plexus:	n/a
16	chr14:35102433-35102483	AoSMC	blood vessel:	n/a
17	chr14:35102433-35102483	NHBE	bronchial:	n/a
18	chr14:35119021-35119071	HUVEC	blood vessel:	n/a
19	chr14:35119021-35119071	Hepatocyte	liver:	n/a
20	chr14:35119021-35119071	HL-60	blood:	n/a
21	chr14:35102433-35102483	AG09319	gingival:	n/a
22	chr14:35119021-35119071	SK-N-SH	brain:	n/a
23	chr14:35102433-35102483	LNCaP	prostate:	n/a
24	chr14:35119021-35119071	AG10803	skin:	n/a
25	chr14:35119021-35119071	MCF10A-Er-Src	breast:	n/a
26	chr14:35102433-35102483	IMR90	lung:	fetal
27	chr14:35102433-35102483	MCF10A-Er-Src	breast:	n/a
28	chr14:35102433-35102483	GM19239	blood:	n/a
29	chr14:35119021-35119071	PFSK-1	brain:	n/a
30	chr14:35119021-35119071	NB4	blood:	n/a
31	chr14:35102433-35102483	HCF	heart:	n/a
32	chr14:35102433-35102483	HCPEpiC	choroid plexus:	n/a
33	chr14:35119021-35119071	IMR90	lung:	fetal
34	chr14:35102433-35102483	NT2-D1	testis:	n/a
35	chr14:35102433-35102483	AG04449	skin:	fetal
36	chr14:35119021-35119071	BE2_C	brain:	n/a
37	chr14:35119021-35119071	K562	blood:	n/a
38	chr14:35119021-35119071	AG09319	gingival:	n/a
39	chr14:35102433-35102483	GM06990	blood:	n/a
40	chr14:35119021-35119071	HNPCEpiC	eye:	n/a
41	chr14:35102433-35102483	A549	lung:	n/a
42	chr14:35119021-35119071	HIPEpiC	eye:	n/a
43	chr14:35102433-35102483	HEK293	kidney:	embryo
44	chr14:35119021-35119071	T-47D	breast:	n/a
45	chr14:35102433-35102483	GM12878	blood:	n/a
46	chr14:35102433-35102483	AG10803	skin:	n/a
47	chr14:35119021-35119071	AG09309	skin:	n/a
48	chr14:35119021-35119071	PANC-1	pancreas:	n/a
49	chr14:35119021-35119071	GM12891	blood:	n/a
50	chr14:35102433-35102483	SK-N-MC	brain:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:35101583..35104569-chr14:35180273..35182776,2	K562	blood:
2	chr14:35021714..35023981-chr14:35099677..35102492,2	MCF-7	breast:
3	chr14:35129877..35132741-chr14:35133755..35136058,2	MCF-7	breast:
4	chr14:35103930..35106002-chr14:35116842..35119484,2	MCF-7	breast:
5	chr14:35099347..35101109-chr14:35116790..35118482,2	K562	blood:
6	chr14:35117978..35120935-chr14:35181287..35183685,2	MCF-7	breast:
7	chr14:35103973..35106509-chr14:35117782..35119447,2	K562	blood:
8	chr14:35103930..35106002-chr14:35116842..35119484,2	MCF-7	breast:
9	chr14:35098574..35101295-chr14:35102833..35104889,3	MCF-7	breast:
10	chr14:35022004..35024254-chr14:35128832..35131570,2	MCF-7	breast:
11	chr14:35107496..35110407-chr14:35118041..35119624,2	MCF-7	breast:
12	chr14:35103956..35105473-chr14:35117782..35120594,2	K562	blood:
13	chr14:35120647..35123453-chr14:35134189..35136107,2	MCF-7	breast:
14	chr14:35023387..35025537-chr14:35125652..35127152,2	MCF-7	breast:
15	chr14:35017489..35019232-chr14:35116363..35118749,2	MCF-7	breast:
16	chr14:35114973..35117245-chr14:35342771..35344725,2	K562	blood:
17	chr14:35098107..35100970-chr14:35116404..35118114,2	MCF-7	breast:
18	chr14:35103973..35106509-chr14:35117782..35119447,2	K562	blood:
19	chr14:35114358..35116141-chr14:35116901..35120753,3	MCF-7	breast:
20	chr14:35114358..35116141-chr14:35116901..35120753,3	MCF-7	breast:
21	chr14:35118550..35121820-chr14:35125434..35129120,4	MCF-7	breast:
22	chr14:35118550..35121820-chr14:35125434..35129120,4	MCF-7	breast:
23	chr14:35130824..35132535-chr14:35133653..35135571,2	K562	blood:
24	chr14:35091495..35095564-chr14:35101048..35103200,4	MCF-7	breast:
25	chr14:35103956..35105473-chr14:35117782..35120594,2	K562	blood:
26	chr14:35107496..35110407-chr14:35118041..35119624,2	MCF-7	breast:
27	chr14:35098892..35100934-chr14:35102376..35104733,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SNX6-1	chr14:35112786-35113062	uc_372_-
2	lnc-SRP54-7	chr14:35112786-35113062	uc_372_+

No data

Variant related genes	Relation type
SNX6	TF binding region
SNX6	CpG island
ENSG00000198604	chromatin interactions
ENSG00000129515	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000165410	chromatin interactions

Extended variants
information (count: 1212 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:1212 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4982192	chr14:35101785-35101786	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs547634338	chr14:35101791-35101792	Enhancers Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs138610629	chr14:35101802-35101803	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs192631283	chr14:35101805-35101806	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs550027597	chr14:35101808-35101809	Weak transcription Enhancers Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs569999328	chr14:35101837-35101838	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs183155885	chr14:35101849-35101850	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs76081026	chr14:35101853-35101854	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs565842054	chr14:35101878-35101879	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs4982193	chr14:35101898-35101899	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147423760	chr14:35101928-35101929	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs574951996	chr14:35101954-35101955	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs4982194	chr14:35101995-35101996	Weak transcription Enhancers Bivalent Enhancer	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs557621682	chr14:35102008-35102009	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs4982195	chr14:35102061-35102062	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs371530236	chr14:35102064-35102065	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544991532	chr14:35102070-35102071	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs113544504	chr14:35102085-35102086	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs375876101	chr14:35102113-35102114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs192055478	chr14:35102183-35102184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs4982196	chr14:35102246-35102247	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs559953109	chr14:35102266-35102267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs561094760	chr14:35102365-35102366	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs575200490	chr14:35102416-35102417	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs529897624	chr14:35102442-35102443	Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs375075300	chr14:35102560-35102561	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs563610634	chr14:35102664-35102665	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs10626428	chr14:35102801-35102802	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs33996574	chr14:35102802-35102803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs200119921	chr14:35102803-35102804	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113895654	chr14:35102821-35102822	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111435873	chr14:35102895-35102896	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs184916515	chr14:35102920-35102921	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs565705070	chr14:35102926-35102927	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs528588696	chr14:35102979-35102980	Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs115524246	chr14:35103006-35103007	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs568599479	chr14:35103042-35103043	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs537659216	chr14:35103054-35103055	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557225201	chr14:35103123-35103124	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs571145157	chr14:35103125-35103126	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs189379939	chr14:35103126-35103127	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs552606756	chr14:35103146-35103147	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs111226550	chr14:35103158-35103159	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs572049201	chr14:35103164-35103165	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs76769752	chr14:35103167-35103168	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs564445682	chr14:35103177-35103178	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554640515	chr14:35103241-35103242	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574411048	chr14:35103253-35103254	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543608394	chr14:35103301-35103302	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs140339666	chr14:35103314-35103315	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
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
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:147 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35099800-35102200	Enhancers	Fetal Intestine Small	intestine
2	chr14:35099800-35103000	Weak transcription	K562	blood
3	chr14:35099800-35104000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:35100000-35103200	Weak transcription	A549	lung
5	chr14:35100000-35103200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr14:35100000-35103800	Weak transcription	NHLF	lung
7	chr14:35101000-35101800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr14:35101600-35101800	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr14:35101600-35101800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr14:35101600-35102000	Enhancers	Hela-S3	cervix
11	chr14:35101600-35102000	Bivalent Enhancer	HepG2	liver
12	chr14:35101800-35102200	Enhancers	Duodenum Mucosa	Duodenum
13	chr14:35102000-35103000	Weak transcription	Hela-S3	cervix
14	chr14:35102200-35103200	Weak transcription	Duodenum Mucosa	Duodenum
15	chr14:35103000-35104400	Enhancers	Hela-S3	cervix
16	chr14:35103000-35104400	Enhancers	K562	blood
17	chr14:35103200-35103800	Enhancers	Monocytes-CD14+_RO01746	blood
18	chr14:35103200-35104000	Enhancers	Duodenum Mucosa	Duodenum
19	chr14:35103200-35104400	Enhancers	A549	lung
20	chr14:35103800-35104000	Enhancers	NHLF	lung
21	chr14:35104000-35104200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr14:35104400-35104600	Weak transcription	A549	lung
23	chr14:35104400-35108600	Weak transcription	Hela-S3	cervix
24	chr14:35108200-35111800	Enhancers	Placenta	Placenta
25	chr14:35108600-35109000	Enhancers	Hela-S3	cervix
26	chr14:35109000-35117000	Weak transcription	Hela-S3	cervix
27	chr14:35110000-35110800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:35110200-35110600	Active TSS	Pancreatic Islets	Pancreatic Islet
29	chr14:35110200-35110800	Enhancers	K562	blood
30	chr14:35110200-35110800	Enhancers	Osteobl	bone
31	chr14:35110400-35110800	Enhancers	A549	lung
32	chr14:35110600-35111000	Enhancers	Fetal Muscle Trunk	muscle
33	chr14:35111600-35112800	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr14:35111600-35113200	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr14:35111800-35117000	Weak transcription	Placenta	Placenta
36	chr14:35113200-35115400	Weak transcription	Monocytes-CD14+_RO01746	blood
37	chr14:35115400-35116200	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr14:35115600-35119200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr14:35115800-35116400	Bivalent Enhancer	HepG2	liver
40	chr14:35116000-35116200	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:35116000-35116400	Enhancers	Skeletal Muscle Female	skeletal muscle
42	chr14:35116200-35116400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr14:35117000-35117600	Bivalent Enhancer	HepG2	liver
44	chr14:35117000-35118000	Enhancers	Hela-S3	cervix
45	chr14:35117000-35121600	Enhancers	Placenta	Placenta
46	chr14:35117600-35117800	Flanking Bivalent TSS/Enh	HepG2	liver
47	chr14:35117600-35118200	Enhancers	A549	lung
48	chr14:35117600-35118200	Enhancers	K562	blood
49	chr14:35117600-35120000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:35117800-35118000	Bivalent/Poised TSS	HepG2	liver

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