Variant report

Variant	esv3373377
Chromosome Location	chr7:149476619-149481017
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:30)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:30 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr7:149480644-149480682	K562	blood:	n/a	n/a
2	CEBPB	chr7:149478262-149478545	K562	blood:	n/a	chr7:149478428-149478441
3	CEBPB	chr7:149478267-149478645	MCF-7	breast:	n/a	chr7:149478428-149478441
4	CEBPB	chr7:149478317-149478589	HepG2	liver:	n/a	chr7:149478428-149478441
5	CEBPB	chr7:149478325-149478436	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr7:149478260-149478531	Hela-S3	cervix:	n/a	chr7:149478428-149478441
7	CHD2	chr7:149480142-149480151	K562	blood:	n/a	n/a
8	ELK1	chr7:149478316-149478394	Hela-S3	cervix:	n/a	n/a
9	HMGN3	chr7:149476189-149476853	K562	blood:	n/a	n/a
10	MAFK	chr7:149479891-149480066	K562	blood:	n/a	n/a
11	MAFK	chr7:149479575-149479678	Hela-S3	cervix:	n/a	n/a
12	MAZ	chr7:149478420-149478506	K562	blood:	n/a	n/a
13	MAZ	chr7:149480778-149480816	K562	blood:	n/a	n/a
14	NFIC	chr7:149477632-149478134	ECC-1	luminal epithelium:	n/a	n/a
15	POLR2A	chr7:149479503-149479536	MCF10A-Er-Src	breast:	n/a	n/a
16	POLR2A	chr7:149477534-149477632	K562	blood:	n/a	n/a
17	POLR2A	chr7:149478713-149478910	MCF10A-Er-Src	breast:	n/a	n/a
18	POLR2A	chr7:149480236-149480239	MCF10A-Er-Src	breast:	n/a	n/a
19	POLR2A	chr7:149477271-149477322	K562	blood:	n/a	n/a
20	POLR2A	chr7:149477094-149477095	MCF10A-Er-Src	breast:	n/a	n/a
21	POLR2A	chr7:149478531-149479122	MCF10A-Er-Src	breast:	n/a	n/a
22	POLR2A	chr7:149477258-149477269	K562	blood:	n/a	n/a
23	POLR2A	chr7:149477403-149477405	K562	blood:	n/a	n/a
24	POLR2A	chr7:149477049-149477065	K562	blood:	n/a	n/a
25	POLR2A	chr7:149477157-149477184	K562	blood:	n/a	n/a
26	RCOR1	chr7:149478260-149478326	K562	blood:	n/a	n/a
27	SMC3	chr7:149478263-149478403	GM12878	blood:	n/a	n/a
28	TCF7L2	chr7:149478569-149478705	Hela-S3	cervix:	n/a	n/a
29	ZBTB7A	chr7:149480771-149480935	K562	blood:	n/a	n/a
30	ZNF263	chr7:149478190-149479157	HEK293-T-REx	kidney:	n/a	chr7:149478205-149478214

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr7:149480305-149480355	PANC-1	pancreas:	n/a
2	chr7:149476924-149476974	GM12892	blood:	n/a
3	chr7:149476924-149476974	CMK	blood:	n/a
4	chr7:149476924-149476974	HMEC	breast:	n/a
5	chr7:149476924-149476974	PFSK-1	brain:	n/a
6	chr7:149476924-149476974	SKMC	muscle:	n/a
7	chr7:149480305-149480355	NT2-D1	testis:	n/a
8	chr7:149476924-149476974	T-47D	breast:	n/a
9	chr7:149476924-149476974	HL-60	blood:	n/a
10	chr7:149476924-149476974	MCF10A-Er-Src	breast:	n/a
11	chr7:149480305-149480355	SK-N-SH	brain:	n/a
12	chr7:149476924-149476974	SAEC	small airway:	n/a
13	chr7:149476924-149476974	HCM	heart:	n/a
14	chr7:149476924-149476974	NT2-D1	testis:	n/a
15	chr7:149476924-149476974	GM12878	blood:	n/a
16	chr7:149480305-149480355	IMR90	lung:	fetal
17	chr7:149476924-149476974	U87	brain:	n/a
18	chr7:149480305-149480355	AoSMC	blood vessel:	n/a
19	chr7:149480305-149480355	MCF-7	breast:	n/a
20	chr7:149480305-149480355	AG10803	skin:	n/a
21	chr7:149480305-149480355	Caco-2	colon:	n/a
22	chr7:149476924-149476974	HRPEpiC	eye:	n/a
23	chr7:149480305-149480355	HepG2	liver:	n/a
24	chr7:149480305-149480355	LNCaP	prostate:	n/a
25	chr7:149480305-149480355	NHDF-neo	bronchial:	n/a
26	chr7:149480305-149480355	SAEC	small airway:	n/a
27	chr7:149476924-149476974	Hela-S3	cervix:	n/a
28	chr7:149476924-149476974	NH-A	brain:	n/a
29	chr7:149480305-149480355	ProgFib	skin:	n/a
30	chr7:149480305-149480355	HPAEpiC	pulmonary alveolar:	n/a
31	chr7:149476924-149476974	PrEC	prostate:	n/a
32	chr7:149476924-149476974	GM06990	blood:	n/a
33	chr7:149476924-149476974	IMR90	lung:	fetal
34	chr7:149476924-149476974	GM12891	blood:	n/a
35	chr7:149476924-149476974	NB4	blood:	n/a
36	chr7:149480305-149480355	PFSK-1	brain:	n/a
37	chr7:149480305-149480355	HAEpiC	amniotic membrane:	n/a
38	chr7:149476924-149476974	H1-hESC	embryonic stem cell:	embryo
39	chr7:149480305-149480355	U87	brain:	n/a
40	chr7:149480305-149480355	AG04450	lung:	fetal
41	chr7:149480305-149480355	HCT-116	colon:	n/a
42	chr7:149476924-149476974	AG04450	lung:	fetal
43	chr7:149480305-149480355	BJ	skin:	n/a
44	chr7:149480305-149480355	HRCEpiC	kidney:	n/a
45	chr7:149480305-149480355	HEEpiC	esophagus:	n/a
46	chr7:149480305-149480355	HRE	kidney:	n/a
47	chr7:149480305-149480355	CMK	blood:	n/a
48	chr7:149480305-149480355	BE2_C	brain:	n/a
49	chr7:149476924-149476974	RPTEC	kidney:	n/a
50	chr7:149480305-149480355	Hepatocyte	liver:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr7:149476551..149479010-chr7:149504345..149507000,2	K562	blood:
2	chr7:149475777..149478196-chr7:149495163..149497885,2	K562	blood:
3	chr7:149479781..149482192-chr7:149551108..149553438,2	MCF-7	breast:
4	chr7:149475035..149477131-chr7:149479756..149481551,3	K562	blood:
5	chr7:149479515..149482094-chr7:149544911..149547463,2	MCF-7	breast:
6	chr7:149475035..149477131-chr7:149479756..149481551,3	K562	blood:
7	chr7:149359595..149361550-chr7:149476876..149478987,2	K562	blood:
8	chr7:149478904..149480912-chr7:149507505..149509845,2	K562	blood:
9	chr7:149437611..149439683-chr7:149477013..149479789,2	K562	blood:
10	chr7:149475188..149477836-chr7:149481672..149483696,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF862-1	chr7:149480195-149480379	ENSG00000197558.7
2	lnc-ZNF862-1	chr7:149479270-149479387	ENSG00000197558.7

No data

Variant related genes	Relation type
SSPO	TF binding region
SSPO	CpG island
ENSG00000106479	chromatin interactions
ENSG00000197558	chromatin interactions

Extended variants
information (count: 281 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:281 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530636602	chr7:149476629-149476630	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs570355405	chr7:149476631-149476632	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs528750495	chr7:149476633-149476634	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs570671640	chr7:149476664-149476665	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs57553723	chr7:149476666-149476667	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs397826817	chr7:149476670-149476671	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs201032059	chr7:149476671-149476672	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs539259796	chr7:149476703-149476704	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs546594693	chr7:149476713-149476714	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs569866191	chr7:149476726-149476727	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537818567	chr7:149476727-149476728	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs114386737	chr7:149476742-149476743	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs115728937	chr7:149476788-149476789	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs534064667	chr7:149476790-149476791	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs117472648	chr7:149476853-149476854	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs577323452	chr7:149476889-149476890	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546091576	chr7:149476924-149476925	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs563163415	chr7:149476933-149476934	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs17172924	chr7:149476949-149476950	Enhancers Weak transcription	CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs367839526	chr7:149477007-149477008	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs561701392	chr7:149477010-149477011	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs183038369	chr7:149477057-149477058	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs150621378	chr7:149477068-149477069	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs564034164	chr7:149477070-149477071	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs533114076	chr7:149477093-149477094	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs368331885	chr7:149477094-149477095	Active TSS Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201063025	chr7:149477103-149477104	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372514824	chr7:149477104-149477105	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569909080	chr7:149477123-149477124	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs376652882	chr7:149477126-149477127	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs115488475	chr7:149477195-149477196	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371182931	chr7:149477196-149477197	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs374730092	chr7:149477218-149477219	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs568165115	chr7:149477219-149477220	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369053347	chr7:149477228-149477229	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188677301	chr7:149477229-149477230	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs570874398	chr7:149477233-149477234	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539996982	chr7:149477240-149477241	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs376579787	chr7:149477241-149477242	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs556510420	chr7:149477245-149477246	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs76449555	chr7:149477246-149477247	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs373181436	chr7:149477304-149477305	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs377694318	chr7:149477307-149477308	Active TSS Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs371267413	chr7:149477339-149477340	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs376308512	chr7:149477343-149477344	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs556098285	chr7:149477385-149477386	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs377374373	chr7:149477392-149477393	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs572030534	chr7:149477393-149477394	Active TSS Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs541041328	chr7:149477401-149477402	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs370293281	chr7:149477410-149477411	Active TSS Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Seminomas	18059402	CNVD
Testicular cancer	18059402	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	19415332	CNVD
Medulloblastoma	21979893	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
T-cell lymphomas	19863542	CNVD
Malaria	21533027	CNVD
Melanoma	18172304	CNVD
Renal cell carcinoma	19461508	CNVD
head and neck squamous cell carcinoma	19289630	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	17952124	CNVD
Wilms tumour	21544195	CNVD
Squamous cell cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	17387387	CNVD
Low-grade fibromyxoid sarcoma	0	CNVD
Oligodendroglial tumors	17285580	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Shwachman-Diamond syndrome	22934832	CNVD
Colorectal cancer	19359472	CNVD
Cutaneous malignant melanoma	17690212	CNVD
Leukemia	17361228	CNVD
Breast cancer	16461572	CNVD
Peripheral t-cell lymphoma	19118030	CNVD
Malignant melanoma	17690212	CNVD
Renal cell carcinoma	18592004	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Multiple myeloma	17550852	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neurodevelopmental disorder	22521361	CNVD
abortions and stillbirths	19751515	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Burkitt''s lymphoma	19759907	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Medulloblastoma	16783165	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Papillary thyroid carcinoma	21436994	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Hodgkin''s lymphoma	18179710	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Myelodysplastic syndrome	17634407	CNVD
Multiple myeloma	16461302	CNVD
Neuroblastoma	18923191	CNVD
Schizophrenia	17646849	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	16864856	CNVD
Autism	20808228	CNVD
Breast cancer	21509527	CNVD
Ovarian cancer	21720365	CNVD
Heart disease	21282601	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Glioblastoma multiforme	17002787	CNVD
Lobular carcinoma	20920651	CNVD
Long-qt syndrome	20920651	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Liver carcinoma	19366792	CNVD
Long-qt syndrome	17576883	CNVD
Bradycardia syndrome	17576883	CNVD
Sudden cardiac death	19188705	CNVD
renal disease	17924346	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:110 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:149471000-149480000	Weak transcription	Brain Substantia Nigra	brain
2	chr7:149473800-149479600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr7:149473800-149534800	Weak transcription	Right Atrium	heart
4	chr7:149474200-149479800	Weak transcription	Primary hematopoietic stem cells	blood
5	chr7:149474400-149479400	Weak transcription	Fetal Lung	lung
6	chr7:149474400-149479400	Weak transcription	Left Ventricle	heart
7	chr7:149474600-149479600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr7:149474600-149480000	Weak transcription	Esophagus	oesophagus
9	chr7:149474800-149479400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr7:149475000-149479600	Weak transcription	Lung	lung
11	chr7:149475000-149480000	Weak transcription	Right Ventricle	heart
12	chr7:149475000-149484400	Weak transcription	Pancreas	Pancrea
13	chr7:149475600-149479400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr7:149475800-149477000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr7:149476200-149477000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr7:149476200-149477200	Enhancers	Spleen	Spleen
17	chr7:149476200-149478000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr7:149476400-149476800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr7:149476400-149480600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr7:149476600-149479400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr7:149476800-149479600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr7:149477000-149477600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr7:149477000-149479400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr7:149477200-149477400	Flanking Active TSS	Spleen	Spleen
25	chr7:149477400-149478000	Enhancers	Spleen	Spleen
26	chr7:149477600-149478000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr7:149477800-149478000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
28	chr7:149477800-149478200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
29	chr7:149478000-149478800	Enhancers	Primary hematopoietic stem cells short term culture	blood
30	chr7:149478000-149479200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr7:149478000-149479400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr7:149478000-149479800	Weak transcription	Spleen	Spleen
33	chr7:149478800-149479200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr7:149479000-149479200	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr7:149479000-149480600	Weak transcription	Gastric	stomach
36	chr7:149479000-149481200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr7:149479200-149480800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr7:149479200-149481200	Enhancers	Breast Myoepithelial Primary Cells	Breast
39	chr7:149479200-149483000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr7:149479400-149479600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
41	chr7:149479400-149480000	Enhancers	Left Ventricle	heart
42	chr7:149479400-149481200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr7:149479400-149481200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chr7:149479400-149481200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr7:149479400-149481200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr7:149479400-149481200	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
47	chr7:149479400-149481200	Enhancers	Fetal Lung	lung
48	chr7:149479600-149479800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr7:149479600-149479800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr7:149479600-149480000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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