Variant report

Variant	esv1821595
Chromosome Location	chr3:138043128-138055402
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:791)
CpG islands
(count:1098)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:791 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:138048098-138048286	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:138051371-138051684	K562	blood:	n/a	n/a
3	ARID3A	chr3:138047265-138047489	K562	blood:	n/a	n/a
4	BACH1	chr3:138048065-138048758	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr3:138047485-138047488	K562	blood:	n/a	n/a
6	BHLHE40	chr3:138048622-138048752	K562	blood:	n/a	n/a
7	BRCA1	chr3:138048783-138048785	HepG2	liver:	n/a	n/a
8	CCNT2	chr3:138048543-138048894	K562	blood:	n/a	n/a
9	CEBPB	chr3:138048698-138048848	HepG2	liver:	n/a	n/a
10	CEBPZ	chr3:138048005-138048006	HepG2	liver:	n/a	n/a
11	CHD1	chr3:138051344-138051768	IMR90	lung:	n/a	n/a
12	CHD1	chr3:138048087-138048636	H1-hESC	embryonic stem cell:	n/a	chr3:138048234-138048243
13	CHD2	chr3:138047901-138048280	H1-hESC	embryonic stem cell:	n/a	chr3:138048234-138048243
14	CHD2	chr3:138048081-138048294	HepG2	liver:	n/a	chr3:138048234-138048243
15	CHD2	chr3:138048121-138048195	GM12878	blood:	n/a	n/a
16	CHD2	chr3:138048571-138048936	H1-hESC	embryonic stem cell:	n/a	n/a
17	CREB1	chr3:138048495-138048910	A549	lung:	n/a	n/a
18	CREB1	chr3:138047989-138048317	A549	lung:	n/a	n/a
19	CREB1	chr3:138048405-138049081	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr3:138047240-138047390	BE2_C	brain:	n/a	n/a
21	CTCF	chr3:138047231-138047457	HepG2	liver:	n/a	n/a
22	CTCF	chr3:138048080-138048230	HVMF	connective:	n/a	n/a
23	CTCF	chr3:138046500-138046650	HCFaa	heart:	n/a	chr3:138046620-138046633
24	CTCF	chr3:138051356-138051618	Lung_OC	lung:	n/a	chr3:138051483-138051496 chr3:138051482-138051503 chr3:138051480-138051498
25	CTCF	chr3:138050160-138050310	HPF	lung:	n/a	chr3:138050227-138050240 chr3:138050224-138050242 chr3:138050226-138050247
26	CTCF	chr3:138051400-138051550	GM12873	blood:	n/a	chr3:138051483-138051496 chr3:138051482-138051503 chr3:138051480-138051498
27	CTCF	chr3:138051445-138051497	GM20000	blood:	n/a	chr3:138051483-138051496
28	CTCF	chr3:138051437-138051546	GM13976	blood:	n/a	chr3:138051483-138051496 chr3:138051482-138051503 chr3:138051480-138051498
29	CTCF	chr3:138048040-138048190	GM12868	blood:	n/a	n/a
30	CTCF	chr3:138048020-138048170	A549	lung:	n/a	n/a
31	CTCF	chr3:138051700-138051850	A549	lung:	n/a	chr3:138051758-138051766
32	CTCF	chr3:138048040-138048190	HFF-Myc	foreskin:	n/a	n/a
33	CTCF	chr3:138047360-138047510	HCT-116	colon:	n/a	n/a
34	CTCF	chr3:138051720-138051870	GM12873	blood:	n/a	chr3:138051758-138051766
35	CTCF	chr3:138051420-138051570	HRPEpiC	eye:	n/a	chr3:138051483-138051496 chr3:138051482-138051503 chr3:138051480-138051498
36	CTCF	chr3:138048013-138048230	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr3:138047320-138047470	AG10803	skin:	n/a	n/a
38	CTCF	chr3:138048080-138048230	GM12866	blood:	n/a	n/a
39	CTCF	chr3:138050140-138050290	HCPEpiC	choroid plexus:	n/a	chr3:138050227-138050240 chr3:138050224-138050242 chr3:138050226-138050247
40	CTCF	chr3:138047202-138047611	MCF-7	breast:	n/a	n/a
41	CTCF	chr3:138050160-138050310	AG09319	gingival:	n/a	chr3:138050227-138050240 chr3:138050224-138050242 chr3:138050226-138050247
42	CTCF	chr3:138048060-138048210	GM12872	blood:	n/a	n/a
43	CTCF	chr3:138051420-138051570	GM12872	blood:	n/a	chr3:138051483-138051496 chr3:138051482-138051503 chr3:138051480-138051498
44	CTCF	chr3:138048060-138048210	GM12875	blood:	n/a	n/a
45	CTCF	chr3:138048060-138048210	BE2_C	brain:	n/a	n/a
46	CTCF	chr3:138048060-138048210	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr3:138048060-138048210	HepG2	liver:	n/a	n/a
48	CTCF	chr3:138047260-138047410	AoAF	blood vessel:	n/a	n/a
49	CTCF	chr3:138048460-138048610	GM12864	blood:	n/a	chr3:138048461-138048471
50	CTCF	chr3:138048080-138048230	K562	blood:	n/a	n/a

(count:1098 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:138048838-138048888	GM12892	blood:	n/a
2	chr3:138048670-138048720	GM12891	blood:	n/a
3	chr3:138048777-138048827	T-47D	breast:	n/a
4	chr3:138043140-138043190	IMR90	lung:	fetal
5	chr3:138048777-138048827	HCF	heart:	n/a
6	chr3:138043797-138043847	AG10803	skin:	n/a
7	chr3:138048777-138048827	H1-hESC	embryonic stem cell:	embryo
8	chr3:138045705-138045755	U87	brain:	n/a
9	chr3:138048777-138048827	SK-N-SH_RA	brain:	n/a
10	chr3:138048777-138048827	HNPCEpiC	eye:	n/a
11	chr3:138043140-138043190	SKMC	muscle:	n/a
12	chr3:138048670-138048720	AG09319	gingival:	n/a
13	chr3:138051670-138051720	ECC-1	luminal epithelium:	n/a
14	chr3:138048101-138048151	LNCaP	prostate:	n/a
15	chr3:138048777-138048827	BJ	skin:	n/a
16	chr3:138043140-138043190	BJ	skin:	n/a
17	chr3:138048746-138048796	ECC-1	luminal epithelium:	n/a
18	chr3:138047362-138047412	AG04449	skin:	fetal
19	chr3:138051670-138051720	HNPCEpiC	eye:	n/a
20	chr3:138043797-138043847	AG09309	skin:	n/a
21	chr3:138048728-138048778	HEK293	kidney:	embryo
22	chr3:138051670-138051720	HCPEpiC	choroid plexus:	n/a
23	chr3:138048335-138048385	AG04449	skin:	fetal
24	chr3:138047362-138047412	LNCaP	prostate:	n/a
25	chr3:138048746-138048796	GM19239	blood:	n/a
26	chr3:138048402-138048452	HUVEC	blood vessel:	n/a
27	chr3:138048728-138048778	HCPEpiC	choroid plexus:	n/a
28	chr3:138048838-138048888	HPAEpiC	pulmonary alveolar:	n/a
29	chr3:138047362-138047412	NHBE	bronchial:	n/a
30	chr3:138043797-138043847	HCPEpiC	choroid plexus:	n/a
31	chr3:138048670-138048720	Hepatocyte	liver:	n/a
32	chr3:138048101-138048151	HIPEpiC	eye:	n/a
33	chr3:138043140-138043190	HAEpiC	amniotic membrane:	n/a
34	chr3:138048370-138048420	HMEC	breast:	n/a
35	chr3:138047362-138047412	H1-hESC	embryonic stem cell:	embryo
36	chr3:138048746-138048796	CMK	blood:	n/a
37	chr3:138048777-138048827	RPTEC	kidney:	n/a
38	chr3:138045705-138045755	T-47D	breast:	n/a
39	chr3:138051670-138051720	GM12891	blood:	n/a
40	chr3:138048402-138048452	SK-N-MC	brain:	n/a
41	chr3:138048838-138048888	PANC-1	pancreas:	n/a
42	chr3:138048937-138048987	T-47D	breast:	n/a
43	chr3:138049011-138049061	Jurkat	blood:	n/a
44	chr3:138048101-138048151	H1-hESC	embryonic stem cell:	embryo
45	chr3:138048335-138048385	ProgFib	skin:	n/a
46	chr3:138048777-138048827	HMEC	breast:	n/a
47	chr3:138045705-138045755	HPAEpiC	pulmonary alveolar:	n/a
48	chr3:138048838-138048888	HEK293	kidney:	embryo
49	chr3:138048777-138048827	SK-N-MC	brain:	n/a
50	chr3:138051670-138051720	SKMC	muscle:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:138051070..138051808-chr3:138136099..138136657,2	MCF-7	breast:
2	chr3:138050301..138052204-chr3:138116487..138117341,9	MCF-7	breast:
3	chr3:138047684..138048542-chr3:138066905..138067491,2	MCF-7	breast:
4	chr3:138049031..138051913-chr3:138117150..138118923,2	MCF-7	breast:
5	chr3:138043371..138046599-chr3:138047282..138051436,3	K562	blood:
6	chr3:138044559..138046647-chr3:138048473..138050103,2	MCF-7	breast:
7	chr3:138051022..138051610-chr3:138144950..138145530,2	MCF-7	breast:
8	chr3:138047736..138050493-chr3:138067682..138070270,2	MCF-7	breast:
9	chr3:138045780..138048564-chr3:138065051..138067433,2	K562	blood:
10	chr3:138043371..138046599-chr3:138047282..138051436,3	K562	blood:
11	chr3:138042389..138044114-chr3:138065779..138068075,2	K562	blood:
12	chr3:137906153..137907747-chr3:138046736..138050249,3	MCF-7	breast:

No data

Variant related genes	Relation type
NME9	TF binding region
NME9	CpG island
ENSG00000181322	chromatin interactions
ENSG00000114098	chromatin interactions
ENSG00000158186	chromatin interactions

Extended variants
information (count: 381 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:381 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74334205	chr3:138043128-138043129	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs574290177	chr3:138043132-138043133	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs542626344	chr3:138043194-138043195	Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs115422641	chr3:138043205-138043206	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs193212653	chr3:138043209-138043210	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs185566254	chr3:138043277-138043278	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs189246416	chr3:138043500-138043501	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs151188181	chr3:138043504-138043505	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs376169959	chr3:138043536-138043537	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs60741176	chr3:138043573-138043574	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs55961241	chr3:138043575-138043576	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs67510531	chr3:138043581-138043582	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs527468092	chr3:138043583-138043584	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs192281231	chr3:138043659-138043660	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs377639124	chr3:138043660-138043661	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs146272669	chr3:138043714-138043715	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs371628363	chr3:138043740-138043741	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs374261419	chr3:138043765-138043766	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs373435345	chr3:138043799-138043800	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs530007029	chr3:138043816-138043817	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs577971960	chr3:138044030-138044031	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs139693574	chr3:138044116-138044117	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs6796118	chr3:138044168-138044169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs80136895	chr3:138044223-138044224	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370759698	chr3:138044240-138044241	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58680542	chr3:138044253-138044254	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs74369810	chr3:138044264-138044265	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs552277135	chr3:138044307-138044308	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs565812017	chr3:138044354-138044355	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs534096632	chr3:138044381-138044382	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs547990538	chr3:138044428-138044429	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs567814581	chr3:138044439-138044440	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs560801108	chr3:138044564-138044565	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536960343	chr3:138044622-138044623	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs201007746	chr3:138044639-138044640	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533902397	chr3:138044720-138044721	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368540924	chr3:138044729-138044730	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs79492841	chr3:138044730-138044731	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs188596826	chr3:138044748-138044749	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538682187	chr3:138044765-138044766	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs558592192	chr3:138044790-138044791	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs75106853	chr3:138044833-138044834	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs554282796	chr3:138044848-138044849	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs115739998	chr3:138044874-138044875	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs540823337	chr3:138044919-138044920	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561147972	chr3:138044969-138044970	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs574588333	chr3:138045047-138045048	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs543701198	chr3:138045057-138045058	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs563605878	chr3:138045081-138045082	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs546101582	chr3:138045085-138045086	Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Multiple myeloma	17550852	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Intracranial aneurysm	16715129	CNVD
Lung cancer	16740712	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Developmental delay	21147756	CNVD
lymphocytic leukemia	21291569	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:138028800-138046600	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr3:138035600-138046800	Weak transcription	Brain Anterior Caudate	brain
3	chr3:138038600-138048200	Weak transcription	Gastric	stomach
4	chr3:138041000-138043400	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr3:138041400-138043400	Enhancers	Primary T cells from cord blood	blood
6	chr3:138041400-138044200	Enhancers	Adipose Nuclei	Adipose
7	chr3:138041400-138047400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:138041600-138044000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr3:138041600-138045200	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr3:138041600-138047400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
11	chr3:138041800-138043200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr3:138041800-138043400	Enhancers	Right Atrium	heart
13	chr3:138041800-138043800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr3:138041800-138047400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr3:138041800-138047400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
16	chr3:138042000-138046600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
17	chr3:138042000-138047400	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr3:138042000-138047400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
19	chr3:138042000-138048000	Weak transcription	Esophagus	oesophagus
20	chr3:138042200-138043200	Enhancers	Fetal Muscle Leg	muscle
21	chr3:138042200-138043400	Enhancers	Psoas Muscle	Psoas
22	chr3:138042200-138047200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
23	chr3:138042400-138043800	Enhancers	Skeletal Muscle Male	skeletal muscle
24	chr3:138042400-138045200	Weak transcription	Placenta	Placenta
25	chr3:138042400-138047400	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr3:138042400-138047400	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr3:138042400-138047400	Enhancers	NHEK	skin
28	chr3:138042600-138043200	Genic enhancers	Brain Dorsolateral Prefrontal Cortex	brain
29	chr3:138042600-138043400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr3:138042600-138044200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr3:138042600-138047400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr3:138042800-138043600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
33	chr3:138042800-138043800	Enhancers	HMEC	breast
34	chr3:138042800-138044000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr3:138042800-138044000	Enhancers	HUVEC	blood vessel
36	chr3:138042800-138044200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr3:138042800-138044200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr3:138042800-138047200	Weak transcription	Brain Hippocampus Middle	brain
39	chr3:138043000-138043200	Enhancers	NH-A	brain
40	chr3:138043000-138043400	Enhancers	K562	blood
41	chr3:138043000-138043600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr3:138043200-138043400	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:138043200-138043400	Enhancers	Brain Substantia Nigra	brain
44	chr3:138043200-138043600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr3:138043200-138046800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
46	chr3:138043400-138044800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:138043400-138047400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr3:138043400-138047400	Weak transcription	K562	blood
49	chr3:138043600-138046400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
50	chr3:138043600-138046800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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