Variant report

Variant	esv3465869
Chromosome Location	chr4:103783563-103787412
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:15)
CpG islands
(count:61)
Chromatin interactive
region (count:16)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:15 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:103786885-103787040	K562	blood:	n/a	n/a
2	EP300	chr4:103787045-103787117	GM12878	blood:	n/a	n/a
3	EP300	chr4:103787169-103787332	K562	blood:	n/a	n/a
4	EP300	chr4:103786692-103787214	K562	blood:	n/a	n/a
5	GATA1	chr4:103786588-103787275	PBDE	blood:	n/a	n/a
6	GATA3	chr4:103783607-103783786	SH-SY5Y	brain:	n/a	n/a
7	JUND	chr4:103786816-103787619	K562	blood:	n/a	n/a
8	POLR2A	chr4:103784290-103784321	MCF-7	breast:	n/a	n/a
9	POLR2A	chr4:103785286-103785360	GM12878	blood:	n/a	n/a
10	RCOR1	chr4:103786805-103786884	GM12878	blood:	n/a	n/a
11	RCOR1	chr4:103786545-103787166	K562	blood:	n/a	n/a
12	RFX5	chr4:103787270-103787274	K562	blood:	n/a	n/a
13	SPI1	chr4:103783061-103783616	HL-60	blood:	n/a	chr4:103783394-103783407 chr4:103783382-103783391 chr4:103783380-103783393 chr4:103783337-103783344 chr4:103783395-103783408 chr4:103783336-103783345 chr4:103783334-103783347 chr4:103783397-103783406
14	TBL1XR1	chr4:103786709-103787219	K562	blood:	n/a	n/a
15	ZNF384	chr4:103786489-103786862	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:103787113-103787163	K562	blood:	n/a
2	chr4:103787113-103787163	HepG2	liver:	n/a
3	chr4:103787113-103787163	MCF-7	breast:	n/a
4	chr4:103787113-103787163	HRE	kidney:	n/a
5	chr4:103787113-103787163	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:103787113-103787163	ECC-1	luminal epithelium:	n/a
7	chr4:103787113-103787163	T-47D	breast:	n/a
8	chr4:103787113-103787163	Hepatocyte	liver:	n/a
9	chr4:103787113-103787163	CMK	blood:	n/a
10	chr4:103787113-103787163	BJ	skin:	n/a
11	chr4:103787113-103787163	PANC-1	pancreas:	n/a
12	chr4:103787113-103787163	SK-N-SH	brain:	n/a
13	chr4:103787113-103787163	RPTEC	kidney:	n/a
14	chr4:103787113-103787163	NT2-D1	testis:	n/a
15	chr4:103787113-103787163	MCF10A-Er-Src	breast:	n/a
16	chr4:103787113-103787163	NHDF-neo	bronchial:	n/a
17	chr4:103787113-103787163	NH-A	brain:	n/a
18	chr4:103787113-103787163	AG04450	lung:	fetal
19	chr4:103787113-103787163	HAEpiC	amniotic membrane:	n/a
20	chr4:103787113-103787163	PFSK-1	brain:	n/a
21	chr4:103787113-103787163	AG04449	skin:	fetal
22	chr4:103787113-103787163	IMR90	lung:	fetal
23	chr4:103787113-103787163	HCM	heart:	n/a
24	chr4:103787113-103787163	H1-hESC	embryonic stem cell:	embryo
25	chr4:103787113-103787163	AG09319	gingival:	n/a
26	chr4:103787113-103787163	GM12892	blood:	n/a
27	chr4:103787113-103787163	AoSMC	blood vessel:	n/a
28	chr4:103787113-103787163	HEK293	kidney:	embryo
29	chr4:103787113-103787163	Caco-2	colon:	n/a
30	chr4:103787113-103787163	HRPEpiC	eye:	n/a
31	chr4:103787113-103787163	HCF	heart:	n/a
32	chr4:103787113-103787163	HEEpiC	esophagus:	n/a
33	chr4:103787113-103787163	HRCEpiC	kidney:	n/a
34	chr4:103787113-103787163	NB4	blood:	n/a
35	chr4:103787113-103787163	AG10803	skin:	n/a
36	chr4:103787113-103787163	ProgFib	skin:	n/a
37	chr4:103787113-103787163	HNPCEpiC	eye:	n/a
38	chr4:103787113-103787163	HUVEC	blood vessel:	n/a
39	chr4:103787113-103787163	HCPEpiC	choroid plexus:	n/a
40	chr4:103787113-103787163	HMEC	breast:	n/a
41	chr4:103787113-103787163	A549	lung:	n/a
42	chr4:103787113-103787163	PrEC	prostate:	n/a
43	chr4:103787113-103787163	HIPEpiC	eye:	n/a
44	chr4:103787113-103787163	BE2_C	brain:	n/a
45	chr4:103787113-103787163	GM06990	blood:	n/a
46	chr4:103787113-103787163	AG09309	skin:	n/a
47	chr4:103787113-103787163	SKMC	muscle:	n/a
48	chr4:103787113-103787163	U87	brain:	n/a
49	chr4:103787113-103787163	GM12891	blood:	n/a
50	chr4:103787113-103787163	SAEC	small airway:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:103746553..103755574-chr4:103787108..103794302,29	MCF-7	breast:
2	chr4:103747316..103751264-chr4:103783852..103786816,4	MCF-7	breast:
3	chr4:103741330..103752134-chr4:103778393..103796398,92	K562	blood:
4	chr4:103767414..103770049-chr4:103783423..103785065,2	MCF-7	breast:
5	chr4:103782734..103784847-chr4:103785870..103787705,2	MCF-7	breast:
6	chr4:103736995..103756245-chr4:103778393..103800311,117	K562	blood:
7	chr4:103782723..103785636-chr4:103787155..103789919,2	MCF-7	breast:
8	chr4:103757925..103760228-chr4:103782951..103785960,3	K562	blood:
9	chr4:103775754..103778384-chr4:103782833..103785617,2	MCF-7	breast:
10	chr4:103781973..103785521-chr4:103788128..103792048,4	MCF-7	breast:
11	chr4:103727572..103730495-chr4:103786922..103788552,2	MCF-7	breast:
12	chr4:103782723..103785636-chr4:103787155..103789919,2	MCF-7	breast:
13	chr4:103746438..103750337-chr4:103782400..103786138,6	MCF-7	breast:
14	chr4:103776066..103778071-chr4:103784776..103786781,2	K562	blood:
15	chr4:103782734..103784847-chr4:103785870..103787705,2	MCF-7	breast:
16	chr4:103770498..103773178-chr4:103786218..103788263,2	K562	blood:

No data

Variant related genes	Relation type
CISD2	TF binding region
ENSG00000238948	TF binding region
CISD2	CpG island
ENSG00000238948	CpG island
ENSG00000145354	chromatin interactions
ENSG00000246560	chromatin interactions
ENSG00000252739	chromatin interactions
ENSG00000109332	chromatin interactions

Extended variants
information (count: 130 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:130 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs548784923	chr4:103783655-103783656	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs574672038	chr4:103783684-103783685	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs542171138	chr4:103783691-103783692	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs183615349	chr4:103783739-103783740	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs369904483	chr4:103783765-103783766	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs9684571	chr4:103783876-103783877	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs186960410	chr4:103783942-103783943	Weak transcription ZNF genes & repeats Enhancers Strong transcription Flanking Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs372742732	chr4:103784061-103784062	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs148905418	chr4:103784172-103784173	Weak transcription ZNF genes & repeats Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs369719595	chr4:103784207-103784208	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs570229505	chr4:103784231-103784232	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs531347643	chr4:103784243-103784244	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs537764488	chr4:103784289-103784290	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs143584610	chr4:103784293-103784294	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs530316133	chr4:103784294-103784295	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs548442116	chr4:103784328-103784329	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs566848173	chr4:103784368-103784369	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs534076906	chr4:103784415-103784416	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs552361639	chr4:103784419-103784420	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs570913457	chr4:103784427-103784428	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs112267706	chr4:103784439-103784440	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs369502158	chr4:103784463-103784464	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs190218825	chr4:103784475-103784476	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs574775143	chr4:103784476-103784477	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs376134341	chr4:103784483-103784484	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs535865262	chr4:103784503-103784504	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs113069616	chr4:103784504-103784505	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs2738924	chr4:103784505-103784506	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs2738925	chr4:103784506-103784507	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs182608560	chr4:103784543-103784544	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs572381075	chr4:103784607-103784608	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs148039680	chr4:103784644-103784645	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs564173713	chr4:103784658-103784659	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs576068158	chr4:103784659-103784660	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs543188544	chr4:103784675-103784676	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs561839052	chr4:103784720-103784721	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs528833636	chr4:103784735-103784736	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs546990489	chr4:103784736-103784737	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs560371521	chr4:103784743-103784744	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs536832096	chr4:103784744-103784745	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs186544925	chr4:103784760-103784761	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs373316729	chr4:103784772-103784773	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs552841730	chr4:103784825-103784826	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs552732384	chr4:103784886-103784887	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs192364818	chr4:103784888-103784889	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs553552759	chr4:103784894-103784895	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs111521637	chr4:103784900-103784901	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs549972852	chr4:103784911-103784912	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs568562055	chr4:103784925-103784926	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs144759203	chr4:103784931-103784932	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:103 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103750800-103788000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:103765000-103783600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:103765400-103788800	Weak transcription	Left Ventricle	heart
4	chr4:103779000-103787600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:103780000-103788000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:103780200-103789200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:103780400-103788800	Weak transcription	Muscle Satellite Cultured Cells	--
8	chr4:103780800-103788000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr4:103781000-103785000	Weak transcription	Primary T cells from cord blood	blood
10	chr4:103781000-103788800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:103781000-103789400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:103781200-103785800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr4:103781200-103788600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr4:103781800-103784400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr4:103781800-103788000	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr4:103781800-103789600	Weak transcription	Fetal Brain Male	brain
17	chr4:103782000-103788000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:103782200-103785000	Weak transcription	Liver	Liver
19	chr4:103782200-103788600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:103782200-103788600	Weak transcription	Fetal Thymus	thymus
21	chr4:103782200-103788800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr4:103782200-103788800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr4:103782400-103784000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:103782400-103784200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr4:103782400-103788800	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr4:103782400-103788800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr4:103782400-103788800	Weak transcription	Fetal Muscle Leg	muscle
28	chr4:103782400-103789200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr4:103782400-103789400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr4:103782600-103783600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:103782600-103784400	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr4:103782600-103788400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr4:103782600-103789000	Weak transcription	Fetal Stomach	stomach
34	chr4:103782800-103784000	Enhancers	Primary neutrophils fromperipheralblood	blood
35	chr4:103782800-103784200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr4:103782800-103785200	Strong transcription	Dnd41	blood
37	chr4:103783000-103784000	Enhancers	Primary B cells from cord blood	blood
38	chr4:103783200-103786600	Weak transcription	Primary hematopoietic stem cells	blood
39	chr4:103783400-103783600	Enhancers	Monocytes-CD14+_RO01746	blood
40	chr4:103783400-103783800	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr4:103783400-103788800	Weak transcription	Sigmoid Colon	Sigmoid Colon
42	chr4:103783600-103784000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr4:103783600-103784200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:103783600-103784800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:103783800-103784400	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr4:103784000-103784600	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr4:103784000-103785800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr4:103784000-103788600	Weak transcription	Primary neutrophils fromperipheralblood	blood
49	chr4:103784000-103788800	Weak transcription	Primary B cells from cord blood	blood
50	chr4:103784200-103785200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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