Variant report

Variant	esv1821875
Chromosome Location	chr4:103810823-103895872
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:139)
CpG islands
(count:62)
Chromatin interactive
region (count:5)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:139 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:103823033-103823354	GM12878	blood:	n/a	n/a
2	CBX3	chr4:103836093-103836257	K562	blood:	n/a	n/a
3	CEBPB	chr4:103834369-103834680	K562	blood:	n/a	chr4:103834541-103834554 chr4:103834540-103834557
4	CEBPB	chr4:103834352-103834604	K562	blood:	n/a	chr4:103834541-103834554 chr4:103834540-103834557
5	CTCF	chr4:103884561-103884633	Medullo	brain:	n/a	chr4:103884611-103884618
6	CTCF	chr4:103834361-103834613	K562	blood:	n/a	chr4:103834469-103834477
7	CTCF	chr4:103834120-103834270	HCPEpiC	choroid plexus:	n/a	n/a
8	CTCF	chr4:103894415-103894467	Lung_OC	lung:	n/a	n/a
9	CTCF	chr4:103854368-103854411	LNCaP	prostate:	n/a	n/a
10	CTCF	chr4:103834236-103834580	A549	lung:	n/a	chr4:103834469-103834477
11	CTCF	chr4:103832580-103832730	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr4:103832600-103832750	GM12874	blood:	n/a	n/a
13	CTCF	chr4:103834420-103834701	K562	blood:	n/a	chr4:103834469-103834477
14	CTCF	chr4:103834296-103834619	K562	blood:	n/a	chr4:103834469-103834477
15	CTCF	chr4:103883202-103883298	GM13976	blood:	n/a	n/a
16	CTCF	chr4:103834348-103834589	A549	lung:	n/a	chr4:103834469-103834477
17	CTCF	chr4:103822411-103822417	GM10266	blood:	n/a	n/a
18	CTCF	chr4:103834346-103834578	A549	lung:	n/a	chr4:103834469-103834477
19	CTCF	chr4:103832580-103832730	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr4:103838184-103838190	GM10248	blood:	n/a	n/a
21	CTCF	chr4:103839789-103839808	LNCaP	prostate:	n/a	n/a
22	CTCF	chr4:103834214-103834650	A549	lung:	n/a	chr4:103834469-103834477
23	E2F4	chr4:103823836-103823972	MCF10A-Er-Src	breast:	n/a	n/a
24	EGR1	chr4:103850399-103850516	K562	blood:	n/a	n/a
25	EP300	chr4:103838094-103838372	GM12878	blood:	n/a	n/a
26	FOS	chr4:103810990-103811726	MCF10A-Er-Src	breast:	n/a	chr4:103811188-103811195
27	FOS	chr4:103810987-103811557	MCF10A-Er-Src	breast:	n/a	chr4:103811188-103811195
28	FOS	chr4:103810987-103811562	MCF10A-Er-Src	breast:	n/a	chr4:103811188-103811195
29	FOS	chr4:103811020-103811535	MCF10A-Er-Src	breast:	n/a	chr4:103811188-103811195
30	FOSL2	chr4:103818692-103818943	HepG2	liver:	n/a	n/a
31	FOSL2	chr4:103822888-103823193	HepG2	liver:	n/a	n/a
32	FOSL2	chr4:103811087-103811536	HepG2	liver:	n/a	chr4:103811188-103811195 chr4:103811266-103811277
33	FOSL2	chr4:103834325-103834653	HepG2	liver:	n/a	n/a
34	FOSL2	chr4:103811117-103811515	HepG2	liver:	n/a	chr4:103811188-103811195 chr4:103811266-103811277
35	FOXA1	chr4:103822088-103822432	HepG2	liver:	n/a	n/a
36	FOXA1	chr4:103840869-103841284	HepG2	liver:	n/a	n/a
37	FOXA1	chr4:103818799-103819117	HepG2	liver:	n/a	n/a
38	FOXA1	chr4:103840909-103841181	HepG2	liver:	n/a	n/a
39	FOXA1	chr4:103840913-103841314	HepG2	liver:	n/a	n/a
40	FOXA1	chr4:103861442-103861685	T-47D	breast:	n/a	n/a
41	FOXA1	chr4:103840821-103841317	HepG2	liver:	n/a	n/a
42	FOXA2	chr4:103840888-103841148	HepG2	liver:	n/a	n/a
43	FOXA2	chr4:103840875-103841313	A549	lung:	n/a	n/a
44	HEY1	chr4:103817222-103817493	K562	blood:	n/a	n/a
45	IRF1	chr4:103867305-103867323	K562	blood:	n/a	n/a
46	JUND	chr4:103838095-103838412	HepG2	liver:	n/a	n/a
47	JUND	chr4:103834353-103834585	HepG2	liver:	n/a	n/a
48	JUND	chr4:103838251-103838374	HepG2	liver:	n/a	n/a
49	JUND	chr4:103869676-103869893	HepG2	liver:	n/a	n/a
50	JUND	chr4:103811207-103811384	HepG2	liver:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:103867628-103867678	AG10803	skin:	n/a
2	chr4:103867628-103867678	AG10803	skin:	n/a
3	chr4:103867628-103867678	H1-hESC	embryonic stem cell:	embryo
4	chr4:103867628-103867678	GM12891	blood:	n/a
5	chr4:103867628-103867678	SK-N-MC	brain:	n/a
6	chr4:103867628-103867678	GM19239	blood:	n/a
7	chr4:103867628-103867678	T-47D	breast:	n/a
8	chr4:103867628-103867678	SK-N-SH	brain:	n/a
9	chr4:103867628-103867678	NT2-D1	testis:	n/a
10	chr4:103867628-103867678	Hepatocyte	liver:	n/a
11	chr4:103867628-103867678	SAEC	small airway:	n/a
12	chr4:103867628-103867678	GM06990	blood:	n/a
13	chr4:103867628-103867678	AG09319	gingival:	n/a
14	chr4:103867628-103867678	PrEC	prostate:	n/a
15	chr4:103867628-103867678	GM12878	blood:	n/a
16	chr4:103867628-103867678	AoSMC	blood vessel:	n/a
17	chr4:103867628-103867678	HCPEpiC	choroid plexus:	n/a
18	chr4:103867628-103867678	HMEC	breast:	n/a
19	chr4:103867628-103867678	SKMC	muscle:	n/a
20	chr4:103867628-103867678	HPAEpiC	pulmonary alveolar:	n/a
21	chr4:103867628-103867678	HCT-116	colon:	n/a
22	chr4:103867628-103867678	MCF-7	breast:	n/a
23	chr4:103867628-103867678	ProgFib	skin:	n/a
24	chr4:103867628-103867678	A549	lung:	n/a
25	chr4:103867628-103867678	HIPEpiC	eye:	n/a
26	chr4:103867628-103867678	HCM	heart:	n/a
27	chr4:103867628-103867678	K562	blood:	n/a
28	chr4:103867628-103867678	HL-60	blood:	n/a
29	chr4:103867628-103867678	NHDF-neo	bronchial:	n/a
30	chr4:103867628-103867678	NH-A	brain:	n/a
31	chr4:103867628-103867678	HNPCEpiC	eye:	n/a
32	chr4:103867628-103867678	HUVEC	blood vessel:	n/a
33	chr4:103867628-103867678	BE2_C	brain:	n/a
34	chr4:103867628-103867678	PFSK-1	brain:	n/a
35	chr4:103867628-103867678	ovcar-3	ovarian:	n/a
36	chr4:103867628-103867678	HRPEpiC	eye:	n/a
37	chr4:103867628-103867678	NB4	blood:	n/a
38	chr4:103867628-103867678	HAEpiC	amniotic membrane:	n/a
39	chr4:103867628-103867678	RPTEC	kidney:	n/a
40	chr4:103867628-103867678	ECC-1	luminal epithelium:	n/a
41	chr4:103867628-103867678	LNCaP	prostate:	n/a
42	chr4:103867628-103867678	AG04450	lung:	fetal
43	chr4:103867628-103867678	HEEpiC	esophagus:	n/a
44	chr4:103867628-103867678	Hela-S3	cervix:	n/a
45	chr4:103867628-103867678	HRCEpiC	kidney:	n/a
46	chr4:103867628-103867678	MCF10A-Er-Src	breast:	n/a
47	chr4:103867628-103867678	AG04449	skin:	fetal
48	chr4:103867628-103867678	IMR90	lung:	fetal
49	chr4:103867628-103867678	NHBE	bronchial:	n/a
50	chr4:103867628-103867678	SK-N-SH_RA	brain:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:103713400..103715221-chr4:103814511..103816662,2	K562	blood:
2	chr4:103747946..103751403-chr4:103826007..103829702,3	K562	blood:
3	chr4:103876539..103878072-chr4:103939783..103942187,2	K562	blood:
4	chr4:103747662..103750581-chr4:103808763..103811614,2	K562	blood:
5	chr4:103802810..103805581-chr4:103812817..103815542,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC9B2-1	chr4:103827693-103827801	NR_047515
2	lnc-SLC9B2-1	chr4:103831596-103831745	NR_047515
3	lnc-SLC9B2-1	chr4:103833165-103833286	NR_047515
4	lnc-SLC9B2-1	chr4:103833165-103833286	NONHSAT097615
5	lnc-SLC9B2-1	chr4:103826671-103826807	NR_047515
6	lnc-SLC9B2-1	chr4:103853281-103853456	NR_047515
7	lnc-CISD2-6	chr4:103817882-103819394	NONHSAT097617
8	lnc-SLC9B2-1	chr4:103811738-103811830	NR_047515
9	lnc-SLC9B2-1	chr4:103832588-103832694	NR_047515

No data

Variant related genes	Relation type
ACTR3BP4	TF binding region
PABPC1P7	TF binding region
SLC9B1	TF binding region
ACTR3BP4	CpG island
PABPC1P7	CpG island
SLC9B1	CpG island
ENSG00000109332	chromatin interactions
ENSG00000246560	chromatin interactions
ENSG00000164037	chromatin interactions

Extended variants
information (count: 2521 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2521 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559232483	chr4:103810839-103810840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs532951253	chr4:103810856-103810857	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs551207619	chr4:103810875-103810876	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs563375888	chr4:103810953-103810954	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs530555552	chr4:103811055-103811056	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs549078128	chr4:103811056-103811057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs74632941	chr4:103811064-103811065	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs567124023	chr4:103811102-103811103	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs534608418	chr4:103811109-103811110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs574330193	chr4:103811127-103811128	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs548072334	chr4:103811132-103811133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs35840247	chr4:103811147-103811148	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373404676	chr4:103811148-103811149	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs199490840	chr4:103811149-103811150	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs113787390	chr4:103811264-103811265	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs541623382	chr4:103811310-103811311	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs566418032	chr4:103811313-103811314	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs540036719	chr4:103811349-103811350	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs223310	chr4:103811377-103811378	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	mRNA abundance
20	rs113008381	chr4:103811384-103811385	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs190765542	chr4:103811408-103811409	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs555830953	chr4:103811442-103811443	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs573910212	chr4:103811455-103811456	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs541067227	chr4:103811457-103811458	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs545747426	chr4:103811466-103811467	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs565303571	chr4:103811515-103811516	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs559218368	chr4:103811585-103811586	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs577542582	chr4:103811603-103811604	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs142131629	chr4:103811611-103811612	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs532358002	chr4:103811613-103811614	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs181627301	chr4:103811619-103811620	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs563305910	chr4:103811668-103811669	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs530754883	chr4:103811677-103811678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs223309	chr4:103811701-103811702	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
35	rs374612556	chr4:103811731-103811732	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs185744666	chr4:103811745-103811746	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
37	rs528084894	chr4:103811746-103811747	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
38	rs559877191	chr4:103811747-103811748	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
39	rs546666948	chr4:103811752-103811753	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
40	rs566358752	chr4:103811854-103811855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs113360567	chr4:103811855-103811856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552069722	chr4:103811864-103811865	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570100789	chr4:103811900-103811901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190561512	chr4:103811979-103811980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370868415	chr4:103811981-103811982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs199492699	chr4:103811998-103811999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112056340	chr4:103812096-103812097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs573842580	chr4:103812117-103812118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs534675590	chr4:103812170-103812171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs570114934	chr4:103812179-103812180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Pancreatic cancer	17952125	CNVD

Chromatin state (count:94 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:103791200-103834800	Weak transcription	Ovary	ovary
2	chr4:103791400-103818600	Weak transcription	HSMMtube	muscle
3	chr4:103792200-103811000	Weak transcription	Osteobl	bone
4	chr4:103792800-103811400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr4:103796400-103811000	Weak transcription	Left Ventricle	heart
6	chr4:103796400-103819800	Weak transcription	Stomach Smooth Muscle	stomach
7	chr4:103798600-103811000	Weak transcription	Primary T cells fromperipheralblood	blood
8	chr4:103798800-103811000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:103799000-103811000	Weak transcription	Primary T cells from cord blood	blood
10	chr4:103799000-103811400	Weak transcription	Fetal Muscle Trunk	muscle
11	chr4:103799000-103812800	Weak transcription	Brain Hippocampus Middle	brain
12	chr4:103799000-103816800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr4:103799000-103817000	Weak transcription	Fetal Stomach	stomach
14	chr4:103799200-103811000	Weak transcription	Fetal Intestine Large	intestine
15	chr4:103799200-103812400	Weak transcription	Fetal Muscle Leg	muscle
16	chr4:103799200-103812400	Weak transcription	Fetal Thymus	thymus
17	chr4:103799200-103817200	Weak transcription	Brain Germinal Matrix	brain
18	chr4:103799200-103819400	Weak transcription	Thymus	Thymus
19	chr4:103799400-103811000	Weak transcription	Primary B cells from cord blood	blood
20	chr4:103799600-103811200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr4:103799600-103812600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr4:103800000-103812600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr4:103800200-103811400	Weak transcription	Primary monocytes fromperipheralblood	blood
24	chr4:103801000-103811000	Weak transcription	Liver	Liver
25	chr4:103801400-103811400	Weak transcription	Fetal Intestine Small	intestine
26	chr4:103803000-103812800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr4:103803800-103817200	Weak transcription	GM12878-XiMat	blood
28	chr4:103804800-103819000	Weak transcription	K562	blood
29	chr4:103805800-103811400	Weak transcription	Stomach Mucosa	stomach
30	chr4:103807000-103811000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr4:103807000-103811000	Weak transcription	Primary hematopoietic stem cells	blood
32	chr4:103807000-103811000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
33	chr4:103807000-103811400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr4:103807000-103811400	Weak transcription	Monocytes-CD14+_RO01746	blood
35	chr4:103807200-103811000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:103808000-103811000	Weak transcription	Dnd41	blood
37	chr4:103808000-103812600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
38	chr4:103810000-103811600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:103810200-103811800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr4:103810400-103812000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr4:103810400-103816800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr4:103810600-103811800	Enhancers	HMEC	breast
43	chr4:103810600-103811800	Enhancers	NHEK	skin
44	chr4:103810800-103811000	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr4:103810800-103811600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:103810800-103811800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr4:103811000-103811200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr4:103811400-103811800	Enhancers	Stomach Mucosa	stomach
49	chr4:103816800-103817000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr4:103816800-103817400	Enhancers	Breast Myoepithelial Primary Cells	Breast

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