Variant report

Variant	nsv525015
Chromosome Location	chr14:24401749-24406306
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:24401880-24402075	K562	blood:	n/a	n/a
2	CCNT2	chr14:24401727-24402112	K562	blood:	n/a	chr14:24401905-24401925
3	CEBPB	chr14:24404572-24404611	HepG2	liver:	n/a	n/a
4	CEBPB	chr14:24405257-24405473	A549	lung:	n/a	n/a
5	CEBPB	chr14:24405179-24405496	HepG2	liver:	n/a	n/a
6	CEBPD	chr14:24401691-24402224	K562	blood:	n/a	n/a
7	CUX1	chr14:24401818-24402023	K562	blood:	n/a	n/a
8	EP300	chr14:24401979-24402044	K562	blood:	n/a	n/a
9	EP300	chr14:24401701-24402176	K562	blood:	n/a	n/a
10	ESR1	chr14:24403033-24403310	ECC-1	luminal epithelium:	n/a	n/a
11	FOXA2	chr14:24405646-24405977	HepG2	liver:	n/a	n/a
12	GATA1	chr14:24400602-24402491	K562	blood:	n/a	chr14:24401944-24401953 chr14:24401940-24401956 chr14:24401940-24401956
13	GATA1	chr14:24401089-24402206	PBDE	blood:	n/a	chr14:24401944-24401953 chr14:24401940-24401956 chr14:24401940-24401956
14	GATA2	chr14:24401788-24402120	K562	blood:	n/a	chr14:24401944-24401953 chr14:24401940-24401956 chr14:24401940-24401956
15	GATA2	chr14:24401794-24402069	K562	blood:	n/a	chr14:24401944-24401953 chr14:24401940-24401956 chr14:24401940-24401956
16	HMGN3	chr14:24401814-24402076	K562	blood:	n/a	n/a
17	HNF4A	chr14:24405593-24406070	HepG2	liver:	n/a	chr14:24405810-24405823 chr14:24405808-24405826 chr14:24405809-24405824 chr14:24405811-24405823 chr14:24405688-24405703 chr14:24405688-24405703 chr14:24405810-24405822 chr14:24405689-24405701 chr14:24405853-24405866 chr14:24405853-24405866 chr14:24405811-24405824 chr14:24405810-24405824 chr14:24405806-24405828 chr14:24405851-24405866
18	HNF4A	chr14:24405525-24406048	HepG2	liver:	n/a	chr14:24405810-24405823 chr14:24405808-24405826 chr14:24405809-24405824 chr14:24405811-24405823 chr14:24405688-24405703 chr14:24405688-24405703 chr14:24405810-24405822 chr14:24405689-24405701 chr14:24405853-24405866 chr14:24405853-24405866 chr14:24405811-24405824 chr14:24405810-24405824 chr14:24405806-24405828 chr14:24405851-24405866
19	HNF4G	chr14:24405434-24406130	HepG2	liver:	n/a	chr14:24405810-24405823 chr14:24405808-24405826 chr14:24405811-24405823 chr14:24405688-24405703 chr14:24405688-24405703 chr14:24405810-24405822 chr14:24405810-24405825 chr14:24405689-24405701 chr14:24405853-24405866 chr14:24405853-24405866 chr14:24405811-24405824 chr14:24405810-24405824 chr14:24405806-24405828
20	HNF4G	chr14:24405527-24406075	HepG2	liver:	n/a	chr14:24405810-24405823 chr14:24405808-24405826 chr14:24405811-24405823 chr14:24405688-24405703 chr14:24405688-24405703 chr14:24405810-24405822 chr14:24405810-24405825 chr14:24405689-24405701 chr14:24405853-24405866 chr14:24405853-24405866 chr14:24405811-24405824 chr14:24405810-24405824 chr14:24405806-24405828
21	IRF1	chr14:24401681-24402057	K562	blood:	n/a	n/a
22	JUND	chr14:24401795-24401992	K562	blood:	n/a	n/a
23	MAFF	chr14:24402364-24402670	HepG2	liver:	n/a	chr14:24402504-24402522
24	MAFF	chr14:24405628-24405935	HepG2	liver:	n/a	n/a
25	MAFF	chr14:24402373-24402662	K562	blood:	n/a	chr14:24402504-24402522
26	MAFK	chr14:24402330-24402677	HepG2	liver:	n/a	chr14:24402505-24402520 chr14:24402500-24402520 chr14:24402505-24402521
27	MAFK	chr14:24402418-24402647	K562	blood:	n/a	chr14:24402505-24402520 chr14:24402500-24402520 chr14:24402505-24402521
28	MAFK	chr14:24405604-24405943	HepG2	liver:	n/a	n/a
29	MAFK	chr14:24402336-24402684	HepG2	liver:	n/a	chr14:24402505-24402520 chr14:24402500-24402520 chr14:24402505-24402521
30	MAFK	chr14:24405627-24405932	HepG2	liver:	n/a	n/a
31	MAFK	chr14:24402379-24402664	IMR90	lung:	n/a	chr14:24402505-24402520 chr14:24402500-24402520 chr14:24402505-24402521
32	MAX	chr14:24402091-24402333	K562	blood:	n/a	n/a
33	MAZ	chr14:24405790-24405793	HepG2	liver:	n/a	n/a
34	MAZ	chr14:24401850-24402230	K562	blood:	n/a	n/a
35	MYC	chr14:24401709-24402341	K562	blood:	n/a	n/a
36	NR2F2	chr14:24401821-24402101	K562	blood:	n/a	n/a
37	PML	chr14:24401678-24402086	K562	blood:	n/a	n/a
38	POLR2A	chr14:24401783-24402014	K562	blood:	n/a	n/a
39	POLR2A	chr14:24402084-24402347	K562	blood:	n/a	n/a
40	RCOR1	chr14:24401761-24402242	K562	blood:	n/a	n/a
41	RFX5	chr14:24401829-24401971	K562	blood:	n/a	chr14:24401850-24401864
42	TAL1	chr14:24401721-24402147	K562	blood:	n/a	chr14:24401907-24401925
43	TBL1XR1	chr14:24401819-24402166	K562	blood:	n/a	n/a
44	TEAD4	chr14:24401735-24402056	K562	blood:	n/a	n/a
45	TEAD4	chr14:24401668-24402384	K562	blood:	n/a	n/a
46	TRIM28	chr14:24401802-24402040	K562	blood:	n/a	n/a
47	ZMIZ1	chr14:24401826-24402121	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:24404827-24404877	NH-A	brain:	n/a
2	chr14:24404827-24404877	NH-A	brain:	n/a
3	chr14:24404827-24404877	ECC-1	luminal epithelium:	n/a
4	chr14:24404084-24404134	ECC-1	luminal epithelium:	n/a
5	chr14:24404295-24404345	HMEC	breast:	n/a
6	chr14:24404827-24404877	NHDF-neo	bronchial:	n/a
7	chr14:24404827-24404877	MCF10A-Er-Src	breast:	n/a
8	chr14:24404827-24404877	AG04450	lung:	fetal
9	chr14:24404084-24404134	Caco-2	colon:	n/a
10	chr14:24404306-24404356	HRCEpiC	kidney:	n/a
11	chr14:24404306-24404356	AG09309	skin:	n/a
12	chr14:24404084-24404134	PFSK-1	brain:	n/a
13	chr14:24404084-24404134	MCF-7	breast:	n/a
14	chr14:24404306-24404356	NH-A	brain:	n/a
15	chr14:24404084-24404134	GM19239	blood:	n/a
16	chr14:24404827-24404877	K562	blood:	n/a
17	chr14:24404827-24404877	BJ	skin:	n/a
18	chr14:24403907-24403957	H1-hESC	embryonic stem cell:	embryo
19	chr14:24404827-24404877	HNPCEpiC	eye:	n/a
20	chr14:24404827-24404877	HCT-116	colon:	n/a
21	chr14:24403907-24403957	GM19239	blood:	n/a
22	chr14:24404295-24404345	H1-hESC	embryonic stem cell:	embryo
23	chr14:24403907-24403957	HIPEpiC	eye:	n/a
24	chr14:24404295-24404345	Caco-2	colon:	n/a
25	chr14:24404084-24404134	NB4	blood:	n/a
26	chr14:24403907-24403957	NHDF-neo	bronchial:	n/a
27	chr14:24404306-24404356	H1-hESC	embryonic stem cell:	embryo
28	chr14:24404306-24404356	BE2_C	brain:	n/a
29	chr14:24404306-24404356	NB4	blood:	n/a
30	chr14:24404295-24404345	SAEC	small airway:	n/a
31	chr14:24404084-24404134	PrEC	prostate:	n/a
32	chr14:24404827-24404877	GM12891	blood:	n/a
33	chr14:24404827-24404877	HRPEpiC	eye:	n/a
34	chr14:24403907-24403957	SK-N-MC	brain:	n/a
35	chr14:24404084-24404134	HEK293	kidney:	embryo
36	chr14:24403907-24403957	T-47D	breast:	n/a
37	chr14:24404084-24404134	SAEC	small airway:	n/a
38	chr14:24404306-24404356	GM12892	blood:	n/a
39	chr14:24404295-24404345	NH-A	brain:	n/a
40	chr14:24404306-24404356	RPTEC	kidney:	n/a
41	chr14:24404306-24404356	AG04449	skin:	fetal
42	chr14:24403907-24403957	MCF-7	breast:	n/a
43	chr14:24403907-24403957	HCF	heart:	n/a
44	chr14:24404827-24404877	Jurkat	blood:	n/a
45	chr14:24404084-24404134	HMEC	breast:	n/a
46	chr14:24404295-24404345	AG04450	lung:	fetal
47	chr14:24403907-24403957	HCPEpiC	choroid plexus:	n/a
48	chr14:24404306-24404356	HRPEpiC	eye:	n/a
49	chr14:24404306-24404356	CMK	blood:	n/a
50	chr14:24404306-24404356	GM19239	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:24195357..24197443-chr14:24399348..24402008,2	MCF-7	breast:
2	chr14:24404663..24407732-chr14:24421458..24424450,4	MCF-7	breast:
3	chr14:24035516..24037456-chr14:24405967..24408124,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRL-2	chr14:24402956-24403160	NONHSAT035951
2	lnc-NRL-2	chr14:24403378-24403777	NONHSAT035951
3	lnc-NRL-2	chr14:24402956-24403160	ENSG00000259334.1
4	lnc-NRL-2	chr14:24403386-24403777	ENSG00000259334.1

Variant related genes	Relation type
ENSG00000197775	TF binding region
LINC00596	TF binding region
ENSG00000197775	CpG island
LINC00596	CpG island
ENSG00000213983	chromatin interactions
ENSG00000157326	chromatin interactions
ENSG00000215256	chromatin interactions

Extended variants
information (count: 182 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:182 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10483284	chr14:24401749-24401750	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182360803	chr14:24401799-24401800	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs539156238	chr14:24401820-24401821	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185116716	chr14:24401834-24401835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs569479780	chr14:24401835-24401836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs151045843	chr14:24401843-24401844	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs554959680	chr14:24401900-24401901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs575113872	chr14:24401904-24401905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs371690085	chr14:24401907-24401908	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371954047	chr14:24401927-24401928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533535365	chr14:24401972-24401973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs553376573	chr14:24401992-24401993	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576498105	chr14:24402030-24402031	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs545502894	chr14:24402032-24402033	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs375282157	chr14:24402051-24402052	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs75024771	chr14:24402064-24402065	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs542333671	chr14:24402102-24402103	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs11623202	chr14:24402121-24402122	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs142252633	chr14:24402128-24402129	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs370150922	chr14:24402143-24402144	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561817874	chr14:24402149-24402150	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs527611317	chr14:24402157-24402158	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs146208456	chr14:24402188-24402189	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs560494242	chr14:24402194-24402195	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs532607586	chr14:24402237-24402238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs111242087	chr14:24402259-24402260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs191064444	chr14:24402273-24402274	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs184055990	chr14:24402284-24402285	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs141344532	chr14:24402308-24402309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs189037687	chr14:24402391-24402392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs150310636	chr14:24402395-24402396	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs534239393	chr14:24402398-24402399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs137979534	chr14:24402418-24402419	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs375855097	chr14:24402437-24402438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs367995709	chr14:24402454-24402455	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs539094520	chr14:24402473-24402474	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555832047	chr14:24402474-24402475	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576123198	chr14:24402475-24402476	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149493864	chr14:24402506-24402507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143863287	chr14:24402566-24402567	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs28705816	chr14:24402578-24402579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374815938	chr14:24402581-24402582	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs8011460	chr14:24402725-24402726	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs541340377	chr14:24402738-24402739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565531725	chr14:24402778-24402779	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs10145131	chr14:24402782-24402783	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs532545782	chr14:24402788-24402789	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs10709597	chr14:24402805-24402806	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546258075	chr14:24402843-24402844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs562820715	chr14:24402844-24402845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

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

Chromatin state (count:105 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:24398400-24403000	Enhancers	Fetal Intestine Small	intestine
2	chr14:24399000-24401800	Enhancers	Liver	Liver
3	chr14:24399200-24402200	Enhancers	Rectal Smooth Muscle	rectum
4	chr14:24399200-24403000	Enhancers	Fetal Intestine Large	intestine
5	chr14:24399200-24408800	Weak transcription	Lung	lung
6	chr14:24399400-24404800	Weak transcription	Pancreas	Pancrea
7	chr14:24399400-24408200	Weak transcription	Left Ventricle	heart
8	chr14:24399400-24410000	Weak transcription	Brain Cingulate Gyrus	brain
9	chr14:24399400-24411000	Weak transcription	Brain Anterior Caudate	brain
10	chr14:24399600-24409000	Weak transcription	Brain Hippocampus Middle	brain
11	chr14:24399600-24409200	Weak transcription	Brain Germinal Matrix	brain
12	chr14:24400000-24408400	Weak transcription	Brain Inferior Temporal Lobe	brain
13	chr14:24400000-24420000	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr14:24400400-24402600	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr14:24400400-24402600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr14:24400400-24402600	Weak transcription	Fetal Lung	lung
17	chr14:24400400-24411800	Weak transcription	HMEC	breast
18	chr14:24400600-24401800	Weak transcription	Ovary	ovary
19	chr14:24400600-24402200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr14:24400600-24402400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr14:24400600-24405600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr14:24400600-24405600	Weak transcription	Adipose Nuclei	Adipose
23	chr14:24400600-24408600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr14:24400600-24408800	Weak transcription	Duodenum Smooth Muscle	Duodenum
25	chr14:24400600-24409600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
26	chr14:24400600-24421000	Weak transcription	Colon Smooth Muscle	Colon
27	chr14:24400800-24401800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr14:24400800-24402400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr14:24400800-24408600	Weak transcription	Stomach Smooth Muscle	stomach
30	chr14:24400800-24409000	Weak transcription	Aorta	Aorta
31	chr14:24401200-24403200	Enhancers	Fetal Stomach	stomach
32	chr14:24401400-24402800	Enhancers	Fetal Kidney	kidney
33	chr14:24401400-24403000	Enhancers	Duodenum Mucosa	Duodenum
34	chr14:24401400-24404000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr14:24401400-24409800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
36	chr14:24401600-24402000	Enhancers	K562	blood
37	chr14:24401600-24404200	Weak transcription	Stomach Mucosa	stomach
38	chr14:24401800-24402800	Weak transcription	Liver	Liver
39	chr14:24401800-24403200	Enhancers	Ovary	ovary
40	chr14:24401800-24409800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr14:24402000-24402200	Flanking Active TSS	K562	blood
42	chr14:24402000-24403200	Enhancers	Fetal Muscle Leg	muscle
43	chr14:24402200-24403200	Enhancers	K562	blood
44	chr14:24402200-24410000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:24402200-24421200	Weak transcription	Rectal Smooth Muscle	rectum
46	chr14:24402400-24403000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr14:24402400-24403000	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr14:24402400-24409800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr14:24402600-24402800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr14:24402600-24403000	Enhancers	Cortex derived primary cultured neurospheres	brain

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