Variant report

Variant	nsv593562
Chromosome Location	chr4:7170562-7191780
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	chr4:7187928-7188138	HepG2	liver:	n/a	n/a
2	CEBPB	chr4:7186098-7186251	HepG2	liver:	n/a	n/a
3	CEBPZ	chr4:7172080-7172092	HepG2	liver:	n/a	n/a
4	CREB1	chr4:7187886-7188118	A549	lung:	n/a	n/a
5	CTCF	chr4:7189060-7189210	HRPEpiC	eye:	n/a	chr4:7189128-7189141
6	CTCF	chr4:7189040-7189190	AG10803	skin:	n/a	chr4:7189128-7189141
7	CTCF	chr4:7189180-7189330	K562	blood:	n/a	n/a
8	CTCF	chr4:7187875-7188113	GM19239	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
9	CTCF	chr4:7191200-7191350	Caco-2	colon:	n/a	n/a
10	CTCF	chr4:7191680-7191830	GM06990	blood:	n/a	n/a
11	CTCF	chr4:7191300-7191450	MCF-7	breast:	n/a	n/a
12	CTCF	chr4:7187940-7188090	GM12864	blood:	n/a	n/a
13	CTCF	chr4:7191660-7191810	SAEC	small airway:	n/a	n/a
14	CTCF	chr4:7187900-7188050	HEEpiC	esophagus:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
15	CTCF	chr4:7187920-7188062	Kidney_OC	kidney:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
16	CTCF	chr4:7187900-7188050	GM12873	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
17	CTCF	chr4:7187920-7188078	GM10266	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
18	CTCF	chr4:7189060-7189210	HA-sp	spinal cord:	n/a	chr4:7189128-7189141
19	CTCF	chr4:7191600-7191750	HEK293	kidney:	n/a	n/a
20	CTCF	chr4:7191532-7191786	T-47D	breast:	n/a	n/a
21	CTCF	chr4:7188080-7188230	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr4:7187892-7188070	T-47D	breast:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
23	CTCF	chr4:7191700-7191850	GM12872	blood:	n/a	n/a
24	CTCF	chr4:7187826-7188130	H1-hESC	embryonic stem cell:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
25	CTCF	chr4:7187820-7188090	NHDF-neo	bronchial:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
26	CTCF	chr4:7187868-7188114	GM12892	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
27	CTCF	chr4:7187880-7188030	HA-sp	spinal cord:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
28	CTCF	chr4:7187940-7188090	HRE	kidney:	n/a	n/a
29	CTCF	chr4:7187940-7188090	GM12871	blood:	n/a	n/a
30	CTCF	chr4:7190940-7191090	AG04449	skin:	n/a	n/a
31	CTCF	chr4:7187920-7188070	AoAF	blood vessel:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
32	CTCF	chr4:7187920-7188070	SK-N-SH_RA	brain:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
33	CTCF	chr4:7191628-7191756	GM12892	blood:	n/a	n/a
34	CTCF	chr4:7187880-7188130	GM12866	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
35	CTCF	chr4:7191664-7191762	GM12878	blood:	n/a	n/a
36	CTCF	chr4:7188984-7189227	K562	blood:	n/a	chr4:7189128-7189141 chr4:7189035-7189043
37	CTCF	chr4:7189040-7189190	K562	blood:	n/a	chr4:7189128-7189141
38	CTCF	chr4:7191640-7191790	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr4:7187867-7188120	MCF-7	breast:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
40	CTCF	chr4:7191580-7191730	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:7187960-7188110	GM12871	blood:	n/a	n/a
42	CTCF	chr4:7191500-7191650	NHEK	skin:	n/a	n/a
43	CTCF	chr4:7187840-7187990	HCT-116	colon:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
44	CTCF	chr4:7187913-7188071	GM13977	blood:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
45	CTCF	chr4:7191574-7191812	MCF-7	breast:	n/a	n/a
46	CTCF	chr4:7191659-7191737	GM12891	blood:	n/a	n/a
47	CTCF	chr4:7187900-7188050	HepG2	liver:	n/a	chr4:7187933-7187946 chr4:7187937-7187946
48	CTCF	chr4:7189440-7189590	HBMEC	blood vessel:	n/a	n/a
49	CTCF	chr4:7191600-7191750	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr4:7189040-7189190	HPAF	blood vessel:	n/a	chr4:7189128-7189141

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7187171-7187221	NB4	blood:	n/a
2	chr4:7187171-7187221	NB4	blood:	n/a
3	chr4:7187171-7187221	ECC-1	luminal epithelium:	n/a
4	chr4:7187328-7187378	GM06990	blood:	n/a
5	chr4:7186138-7186188	SK-N-SH	brain:	n/a
6	chr4:7187171-7187221	Hela-S3	cervix:	n/a
7	chr4:7185164-7185214	NB4	blood:	n/a
8	chr4:7186138-7186188	HRE	kidney:	n/a
9	chr4:7187171-7187221	U87	brain:	n/a
10	chr4:7187328-7187378	AG04449	skin:	fetal
11	chr4:7185889-7185939	Jurkat	blood:	n/a
12	chr4:7187328-7187378	SK-N-SH	brain:	n/a
13	chr4:7187328-7187378	HEK293	kidney:	embryo
14	chr4:7186138-7186188	AG04450	lung:	fetal
15	chr4:7186138-7186188	AG10803	skin:	n/a
16	chr4:7187171-7187221	ovcar-3	ovarian:	n/a
17	chr4:7185164-7185214	Caco-2	colon:	n/a
18	chr4:7187328-7187378	NHDF-neo	bronchial:	n/a
19	chr4:7184654-7184704	HCT-116	colon:	n/a
20	chr4:7184654-7184704	NT2-D1	testis:	n/a
21	chr4:7187171-7187221	HCM	heart:	n/a
22	chr4:7187328-7187378	K562	blood:	n/a
23	chr4:7185889-7185939	NH-A	brain:	n/a
24	chr4:7186138-7186188	GM12878	blood:	n/a
25	chr4:7185889-7185939	NHBE	bronchial:	n/a
26	chr4:7186138-7186188	NT2-D1	testis:	n/a
27	chr4:7186138-7186188	U87	brain:	n/a
28	chr4:7186138-7186188	SK-N-MC	brain:	n/a
29	chr4:7185164-7185214	HEK293	kidney:	embryo
30	chr4:7186138-7186188	A549	lung:	n/a
31	chr4:7185889-7185939	AoSMC	blood vessel:	n/a
32	chr4:7185164-7185214	BJ	skin:	n/a
33	chr4:7184654-7184704	ovcar-3	ovarian:	n/a
34	chr4:7185164-7185214	BE2_C	brain:	n/a
35	chr4:7185889-7185939	AG04450	lung:	fetal
36	chr4:7185889-7185939	GM12891	blood:	n/a
37	chr4:7187328-7187378	A549	lung:	n/a
38	chr4:7185164-7185214	HMEC	breast:	n/a
39	chr4:7187328-7187378	AG10803	skin:	n/a
40	chr4:7185164-7185214	HCF	heart:	n/a
41	chr4:7184654-7184704	HCF	heart:	n/a
42	chr4:7185164-7185214	HCM	heart:	n/a
43	chr4:7187328-7187378	SAEC	small airway:	n/a
44	chr4:7187171-7187221	HMEC	breast:	n/a
45	chr4:7185164-7185214	HL-60	blood:	n/a
46	chr4:7187328-7187378	NB4	blood:	n/a
47	chr4:7184654-7184704	HRE	kidney:	n/a
48	chr4:7186138-7186188	HepG2	liver:	n/a
49	chr4:7186138-7186188	HRPEpiC	eye:	n/a
50	chr4:7186138-7186188	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:7191464..7193621-chr4:7207783..7210598,2	MCF-7	breast:
2	chr4:7170575..7172996-chr4:7179546..7181445,2	MCF-7	breast:
3	chr4:7170575..7172996-chr4:7179546..7181445,2	MCF-7	breast:
4	chr4:7156869..7158917-chr4:7168840..7170668,2	K562	blood:
5	chr4:7190742..7191404-chr4:7337213..7337934,2	MCF-7	breast:
6	chr4:7179927..7181981-chr4:7190221..7193171,2	MCF-7	breast:
7	chr4:7182824..7185399-chr4:7186079..7187991,2	K562	blood:
8	chr4:7179927..7181981-chr4:7190221..7193171,2	MCF-7	breast:
9	chr4:7153261..7154139-chr4:7187520..7188707,6	MCF-7	breast:
10	chr4:7153303..7154007-chr4:7189364..7189997,2	MCF-7	breast:
11	chr4:7182824..7185399-chr4:7186079..7187991,2	K562	blood:

Variant related genes	Relation type
SORCS2	TF binding region
SORCS2	CpG island

Extended variants
information (count: 1022 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1022 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9991298	chr4:7170562-7170563	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs74797475	chr4:7170588-7170589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs372393516	chr4:7170592-7170593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182683270	chr4:7170626-7170627	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143094204	chr4:7170659-7170660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs527391447	chr4:7170668-7170669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs368501408	chr4:7170675-7170676	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs561156325	chr4:7170692-7170693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79171685	chr4:7170736-7170737	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375925434	chr4:7170743-7170744	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs115464336	chr4:7170751-7170752	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs372866720	chr4:7170781-7170782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs13130611	chr4:7170786-7170787	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs532596991	chr4:7170798-7170799	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369208531	chr4:7170830-7170831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146664053	chr4:7170834-7170835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371591038	chr4:7170939-7170940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536774657	chr4:7170987-7170988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs368867459	chr4:7171008-7171009	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554831055	chr4:7171034-7171035	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs376148283	chr4:7171055-7171056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs532144031	chr4:7171112-7171113	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs570266610	chr4:7171114-7171115	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs566491307	chr4:7171126-7171127	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537324966	chr4:7171135-7171136	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs558872261	chr4:7171196-7171197	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs577210877	chr4:7171197-7171198	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs544561330	chr4:7171234-7171235	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs186954223	chr4:7171238-7171239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533753961	chr4:7171249-7171250	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140256218	chr4:7171253-7171254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs542721655	chr4:7171285-7171286	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs190611905	chr4:7171306-7171307	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111876358	chr4:7171316-7171317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs543347979	chr4:7171351-7171352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs369373901	chr4:7171352-7171353	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs565218256	chr4:7171373-7171374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs547312720	chr4:7171382-7171383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs4689621	chr4:7171386-7171387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs182959264	chr4:7171387-7171388	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138147688	chr4:7171388-7171389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs141717677	chr4:7171389-7171390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs570149542	chr4:7171390-7171391	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs537693214	chr4:7171394-7171395	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs558738311	chr4:7171398-7171399	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs150136555	chr4:7171400-7171401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs369777241	chr4:7171427-7171428	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs373986968	chr4:7171431-7171432	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs572039891	chr4:7171436-7171437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs188538458	chr4:7171442-7171443	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:60 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7105800-7176000	Weak transcription	Right Atrium	heart
2	chr4:7161000-7172800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr4:7162800-7172800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:7167400-7170600	Enhancers	Fetal Intestine Large	intestine
5	chr4:7167400-7170600	Enhancers	Fetal Intestine Small	intestine
6	chr4:7167800-7182800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:7169000-7171200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr4:7169400-7170800	Weak transcription	Esophagus	oesophagus
9	chr4:7170000-7172400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr4:7170400-7171000	Enhancers	Spleen	Spleen
11	chr4:7170400-7171400	Enhancers	Primary B cells from peripheral blood	blood
12	chr4:7170800-7171400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr4:7170800-7172000	Enhancers	Primary T cells fromperipheralblood	blood
14	chr4:7171000-7171200	Enhancers	Esophagus	oesophagus
15	chr4:7172000-7173600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:7172800-7173400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr4:7172800-7173600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr4:7173000-7173200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr4:7173000-7173400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:7173000-7173400	Enhancers	Osteobl	bone
21	chr4:7173400-7174400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:7174400-7175200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:7174800-7175200	Bivalent Enhancer	HepG2	liver
24	chr4:7174800-7175800	Enhancers	Brain Germinal Matrix	brain
25	chr4:7175400-7175600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:7178400-7178800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr4:7182600-7183200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:7182800-7183400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr4:7182800-7183400	Enhancers	Fetal Stomach	stomach
30	chr4:7183400-7187400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:7184600-7185400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr4:7185000-7186000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:7186000-7186600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:7186600-7186800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:7186800-7187200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:7187400-7188600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr4:7187400-7188800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr4:7188000-7189400	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:7188400-7188800	Bivalent Enhancer	Fetal Brain Female	brain
40	chr4:7188400-7189200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr4:7188600-7192800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:7188800-7189200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr4:7189000-7189200	Enhancers	Fetal Brain Male	brain
44	chr4:7189000-7190400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:7189200-7189600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:7189600-7190400	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr4:7190200-7190400	Enhancers	Pancreas	Pancrea
48	chr4:7190400-7191400	Weak transcription	Pancreas	Pancrea
49	chr4:7191000-7191200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
50	chr4:7191200-7191400	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links