Variant report

Variant	esv19608
Chromosome Location	chr13:95253055-95253914
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	chr13:95253882-95254160	K562	blood:	n/a	n/a
2	ATF2	chr13:95253759-95254143	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr13:95253575-95254616	GM12878	blood:	n/a	chr13:95254102-95254118 chr13:95254127-95254143 chr13:95254392-95254408 chr13:95254128-95254144 chr13:95254123-95254139
4	BHLHE40	chr13:95253651-95254395	K562	blood:	n/a	chr13:95254102-95254118 chr13:95254127-95254143 chr13:95254128-95254144 chr13:95254123-95254139
5	CBX3	chr13:95253636-95254002	K562	blood:	n/a	n/a
6	CBX3	chr13:95253520-95254727	HCT-116	colon:	n/a	n/a
7	CBX3	chr13:95253512-95254519	K562	blood:	n/a	n/a
8	CCNT2	chr13:95253720-95254645	K562	blood:	n/a	chr13:95254335-95254344 chr13:95254593-95254602
9	CEBPB	chr13:95253829-95254164	MCF-7	breast:	n/a	chr13:95254055-95254063
10	CEBPB	chr13:95253680-95254080	K562	blood:	n/a	chr13:95254055-95254063
11	CEBPB	chr13:95253722-95254066	A549	lung:	n/a	chr13:95254055-95254063
12	CEBPB	chr13:95253712-95254111	K562	blood:	n/a	chr13:95254055-95254063
13	CEBPB	chr13:95253723-95254102	IMR90	lung:	n/a	chr13:95254055-95254063
14	CEBPB	chr13:95253729-95254172	Hela-S3	cervix:	n/a	chr13:95254055-95254063
15	CEBPB	chr13:95253814-95253977	K562	blood:	n/a	n/a
16	CEBPB	chr13:95253712-95254582	H1-hESC	embryonic stem cell:	n/a	chr13:95254055-95254063
17	CEBPB	chr13:95253704-95254135	MCF-7	breast:	n/a	chr13:95254055-95254063
18	CEBPB	chr13:95253698-95254150	A549	lung:	n/a	chr13:95254055-95254063
19	CHD1	chr13:95253710-95254288	GM12878	blood:	n/a	chr13:95254123-95254133
20	CHD2	chr13:95253668-95254660	GM12878	blood:	n/a	chr13:95254336-95254346 chr13:95254123-95254133
21	CHD2	chr13:95253645-95254676	H1-hESC	embryonic stem cell:	n/a	chr13:95254336-95254346 chr13:95254123-95254133
22	CHD2	chr13:95253722-95254242	K562	blood:	n/a	chr13:95254123-95254133
23	CHD2	chr13:95253755-95254595	Hela-S3	cervix:	n/a	chr13:95254336-95254346 chr13:95254123-95254133
24	CREB1	chr13:95253756-95254368	A549	lung:	n/a	n/a
25	CREB1	chr13:95253761-95254610	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr13:95253853-95254213	ECC-1	luminal epithelium:	n/a	n/a
27	CREB1	chr13:95253699-95254446	GM12878	blood:	n/a	n/a
28	CREB1	chr13:95253656-95254668	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:95253774-95253946	K562	blood:	n/a	n/a
30	E2F1	chr13:95253908-95254551	Hela-S3	cervix:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95254335-95254347 chr13:95254098-95254107
31	E2F4	chr13:95253719-95254536	K562	blood:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95254335-95254347 chr13:95254098-95254107
32	E2F4	chr13:95253747-95253947	GM12878	blood:	n/a	n/a
33	E2F4	chr13:95253672-95254523	MCF10A-Er-Src	breast:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95254335-95254347 chr13:95254098-95254107
34	E2F6	chr13:95253560-95254614	K562	blood:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
35	E2F6	chr13:95253559-95254402	A549	lung:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
36	E2F6	chr13:95253551-95254475	K562	blood:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
37	E2F6	chr13:95253123-95254820	H1-hESC	embryonic stem cell:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95253532-95253541 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
38	E2F6	chr13:95253565-95254228	K562	blood:	n/a	chr13:95254130-95254140 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254098-95254107
39	E2F6	chr13:95253505-95254722	A549	lung:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95253532-95253541 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
40	E2F6	chr13:95253606-95254562	Hela-S3	cervix:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
41	E2F6	chr13:95253255-95254708	H1-hESC	embryonic stem cell:	n/a	chr13:95254335-95254344 chr13:95254130-95254140 chr13:95253532-95253541 chr13:95254137-95254147 chr13:95253880-95253891 chr13:95254335-95254347 chr13:95254098-95254107
42	EBF1	chr13:95253720-95253933	GM12878	blood:	n/a	n/a
43	ELF1	chr13:95253902-95254313	K562	blood:	n/a	n/a
44	ELF1	chr13:95253685-95254500	GM12878	blood:	n/a	n/a
45	ELF1	chr13:95253716-95254697	GM12878	blood:	n/a	n/a
46	ELF1	chr13:95253761-95254128	K562	blood:	n/a	n/a
47	ELK1	chr13:95253180-95253346	Hela-S3	cervix:	n/a	n/a
48	ELK1	chr13:95253884-95254090	Hela-S3	cervix:	n/a	n/a
49	ELK1	chr13:95253674-95254066	GM12878	blood:	n/a	n/a
50	ELK1	chr13:95253699-95253716	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:95253641-95253691	AG10803	skin:	n/a
2	chr13:95253641-95253691	Hela-S3	cervix:	n/a
3	chr13:95253641-95253691	MCF10A-Er-Src	breast:	n/a
4	chr13:95253670-95253720	Caco-2	colon:	n/a
5	chr13:95253670-95253720	HCF	heart:	n/a
6	chr13:95253676-95253726	H1-hESC	embryonic stem cell:	embryo
7	chr13:95253676-95253726	HCPEpiC	choroid plexus:	n/a
8	chr13:95253670-95253720	PANC-1	pancreas:	n/a
9	chr13:95253900-95253950	RPTEC	kidney:	n/a
10	chr13:95253641-95253691	LNCaP	prostate:	n/a
11	chr13:95253900-95253950	NHDF-neo	bronchial:	n/a
12	chr13:95253900-95253950	MCF10A-Er-Src	breast:	n/a
13	chr13:95253676-95253726	HRPEpiC	eye:	n/a
14	chr13:95253641-95253691	PFSK-1	brain:	n/a
15	chr13:95253676-95253726	HRE	kidney:	n/a
16	chr13:95253670-95253720	IMR90	lung:	fetal
17	chr13:95253676-95253726	HL-60	blood:	n/a
18	chr13:95253900-95253950	HMEC	breast:	n/a
19	chr13:95253900-95253950	MCF-7	breast:	n/a
20	chr13:95253676-95253726	MCF10A-Er-Src	breast:	n/a
21	chr13:95253676-95253726	PrEC	prostate:	n/a
22	chr13:95253641-95253691	AG09309	skin:	n/a
23	chr13:95253900-95253950	HRE	kidney:	n/a
24	chr13:95253676-95253726	Jurkat	blood:	n/a
25	chr13:95253676-95253726	BJ	skin:	n/a
26	chr13:95253641-95253691	SAEC	small airway:	n/a
27	chr13:95253670-95253720	BE2_C	brain:	n/a
28	chr13:95253676-95253726	HepG2	liver:	n/a
29	chr13:95253900-95253950	HRPEpiC	eye:	n/a
30	chr13:95253670-95253720	SK-N-SH_RA	brain:	n/a
31	chr13:95253900-95253950	NHBE	bronchial:	n/a
32	chr13:95253641-95253691	HCF	heart:	n/a
33	chr13:95253670-95253720	SK-N-MC	brain:	n/a
34	chr13:95253900-95253950	CMK	blood:	n/a
35	chr13:95253900-95253950	PrEC	prostate:	n/a
36	chr13:95253900-95253950	AoSMC	blood vessel:	n/a
37	chr13:95253641-95253691	AG09319	gingival:	n/a
38	chr13:95253900-95253950	T-47D	breast:	n/a
39	chr13:95253900-95253950	HEK293	kidney:	embryo
40	chr13:95253641-95253691	ovcar-3	ovarian:	n/a
41	chr13:95253641-95253691	SKMC	muscle:	n/a
42	chr13:95253641-95253691	HRCEpiC	kidney:	n/a
43	chr13:95253900-95253950	Hepatocyte	liver:	n/a
44	chr13:95253641-95253691	GM12892	blood:	n/a
45	chr13:95253670-95253720	HCT-116	colon:	n/a
46	chr13:95253641-95253691	BE2_C	brain:	n/a
47	chr13:95253641-95253691	NB4	blood:	n/a
48	chr13:95253676-95253726	HCT-116	colon:	n/a
49	chr13:95253670-95253720	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:95253676-95253726	HPAEpiC	pulmonary alveolar:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:95246267..95250128-chr13:95251933..95256020,6	MCF-7	breast:
2	chr13:95200950..95203234-chr13:95251840..95253410,2	MCF-7	breast:
3	chr13:95247274..95249727-chr13:95251841..95255221,4	MCF-7	breast:
4	chr13:95245952..95249992-chr13:95252491..95255739,5	K562	blood:

Variant related genes	Relation type
GPR180	TF binding region
TGDS	TF binding region
GPR180	CpG island
TGDS	CpG island
ENSG00000088451	chromatin interactions

Extended variants
information (count: 30 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs532817646	chr13:95253100-95253101	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs183382692	chr13:95253103-95253104	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs200923445	chr13:95253125-95253126	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs4995268	chr13:95253126-95253127	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs9561643	chr13:95253131-95253132	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs114471330	chr13:95253151-95253152	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs565602803	chr13:95253195-95253196	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs534587675	chr13:95253196-95253197	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs115034806	chr13:95253208-95253209	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs187706439	chr13:95253230-95253231	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs146715589	chr13:95253301-95253302	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs539488954	chr13:95253302-95253303	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs55726564	chr13:95253315-95253316	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs55664539	chr13:95253327-95253328	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs367895297	chr13:95253366-95253367	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs556953613	chr13:95253419-95253420	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs6492719	chr13:95253474-95253475	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs35636256	chr13:95253493-95253494	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs71111539	chr13:95253506-95253507	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs372294337	chr13:95253511-95253512	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs191852286	chr13:95253537-95253538	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs9590042	chr13:95253542-95253543	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs78563325	chr13:95253565-95253566	Weak transcription Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs116133290	chr13:95253614-95253615	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs562284092	chr13:95253685-95253686	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs554810570	chr13:95253700-95253701	Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541689977	chr13:95253809-95253810	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs574878892	chr13:95253833-95253834	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs75996929	chr13:95253840-95253841	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549522767	chr13:95253854-95253855	Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:235 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95248800-95253200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:95248800-95253200	Weak transcription	Primary T cells from cord blood	blood
3	chr13:95248800-95253600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr13:95248800-95253600	Weak transcription	HUVEC	blood vessel
5	chr13:95249000-95253200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr13:95249000-95253200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr13:95249000-95253200	Weak transcription	Primary neutrophils fromperipheralblood	blood
8	chr13:95249000-95253200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr13:95249000-95253200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr13:95249000-95253200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr13:95249000-95253200	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr13:95249000-95253200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
13	chr13:95249000-95253200	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr13:95249000-95253200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr13:95249000-95253200	Weak transcription	Brain Anterior Caudate	brain
16	chr13:95249000-95253200	Weak transcription	Brain Cingulate Gyrus	brain
17	chr13:95249000-95253200	Weak transcription	Brain Substantia Nigra	brain
18	chr13:95249000-95253200	Weak transcription	Colon Smooth Muscle	Colon
19	chr13:95249000-95253200	Weak transcription	Fetal Brain Male	brain
20	chr13:95249000-95253200	Weak transcription	Fetal Heart	heart
21	chr13:95249000-95253200	Weak transcription	Fetal Kidney	kidney
22	chr13:95249000-95253200	Weak transcription	Fetal Stomach	stomach
23	chr13:95249000-95253200	Weak transcription	Rectal Smooth Muscle	rectum
24	chr13:95249000-95253200	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr13:95249000-95253200	Weak transcription	Osteobl	bone
26	chr13:95249000-95253600	Weak transcription	Primary monocytes fromperipheralblood	blood
27	chr13:95249000-95253600	Weak transcription	Primary hematopoietic stem cells	blood
28	chr13:95249000-95253600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr13:95249000-95253600	Weak transcription	Primary T helper cells fromperipheralblood	blood
30	chr13:95249000-95253600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr13:95249000-95253600	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr13:95249000-95253600	Weak transcription	Adipose Nuclei	Adipose
33	chr13:95249000-95253600	Weak transcription	Fetal Muscle Trunk	muscle
34	chr13:95249000-95253600	Weak transcription	Right Atrium	heart
35	chr13:95249000-95253600	Weak transcription	Monocytes-CD14+_RO01746	blood
36	chr13:95249000-95253800	Weak transcription	Spleen	Spleen
37	chr13:95249200-95253200	Weak transcription	Primary T cells fromperipheralblood	blood
38	chr13:95249200-95253200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
39	chr13:95249200-95253200	Weak transcription	Brain Inferior Temporal Lobe	brain
40	chr13:95249200-95253200	Weak transcription	Placenta	Placenta
41	chr13:95249200-95253200	Weak transcription	Fetal Thymus	thymus
42	chr13:95249200-95253600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr13:95249200-95253600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr13:95249200-95253600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:95249200-95253600	Weak transcription	Colonic Mucosa	Colon
46	chr13:95249200-95253600	Weak transcription	NHEK	skin
47	chr13:95250600-95253600	Weak transcription	NHLF	lung
48	chr13:95251000-95253600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr13:95252000-95253200	Enhancers	HepG2	liver
50	chr13:95252000-95253400	Enhancers	Stomach Mucosa	stomach

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