Variant report

Variant	nsv946423
Chromosome Location	chr1:155732243-155737328
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:142)
CpG islands
(count:0)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:142 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL3	chr1:155733349-155733580	GM12878	blood:	n/a	chr1:155733478-155733487
2	CEBPB	chr1:155733895-155734057	IMR90	lung:	n/a	n/a
3	CEBPB	chr1:155733315-155733613	A549	lung:	n/a	n/a
4	CEBPB	chr1:155733260-155733666	MCF-7	breast:	n/a	n/a
5	CEBPB	chr1:155733274-155733671	A549	lung:	n/a	n/a
6	CEBPB	chr1:155733212-155733670	A549	lung:	n/a	n/a
7	CEBPB	chr1:155733314-155733512	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr1:155733312-155733671	IMR90	lung:	n/a	n/a
9	CTCF	chr1:155733310-155733421	Fibrobl	skin:	n/a	n/a
10	CTCF	chr1:155733308-155733424	NHEK	skin:	n/a	n/a
11	CTCF	chr1:155733305-155733425	LNCaP	prostate:	n/a	n/a
12	CTCF	chr1:155733300-155733468	MCF-7	breast:	n/a	n/a
13	CTCF	chr1:155733152-155733476	A549	lung:	n/a	n/a
14	CTCF	chr1:155736079-155736132	MCF-7	breast:	n/a	n/a
15	CTCF	chr1:155733320-155733447	ProgFib	skin:	n/a	n/a
16	CTCF	chr1:155733304-155733500	IMR90	lung:	n/a	n/a
17	CTCF	chr1:155733322-155733437	Hela-S3	cervix:	n/a	n/a
18	CTCF	chr1:155733314-155733436	K562	blood:	n/a	n/a
19	CTCF	chr1:155733180-155733330	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr1:155733306-155733452	Gliobla	brain:	n/a	n/a
21	CTCF	chr1:155733267-155733418	A549	lung:	n/a	n/a
22	CTCF	chr1:155736064-155736143	HepG2	liver:	n/a	n/a
23	CTCF	chr1:155733312-155733474	HUVEC	blood vessel:	n/a	n/a
24	CTCF	chr1:155733303-155733419	A549	lung:	n/a	n/a
25	CTCF	chr1:155733328-155733414	MCF-7	breast:	n/a	n/a
26	CTCF	chr1:155733325-155733448	HepG2	liver:	n/a	n/a
27	CTCF	chr1:155736057-155736111	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr1:155733316-155733484	K562	blood:	n/a	n/a
29	CTCF	chr1:155733145-155733575	A549	lung:	n/a	n/a
30	CTCF	chr1:155733309-155733367	Medullo	brain:	n/a	n/a
31	CTCF	chr1:155733257-155733360	HepG2	liver:	n/a	n/a
32	CTCF	chr1:155733180-155733330	HMF	breast:	n/a	n/a
33	CTCF	chr1:155733180-155733330	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr1:155736067-155736105	K562	blood:	n/a	n/a
35	CTCF	chr1:155733180-155733330	HCM	heart:	n/a	n/a
36	CTCF	chr1:155733299-155733407	LNCaP	prostate:	n/a	n/a
37	CTCF	chr1:155733345-155733400	GM12878	blood:	n/a	n/a
38	CTCF	chr1:155733094-155733439	A549	lung:	n/a	n/a
39	CTCF	chr1:155733272-155733444	A549	lung:	n/a	n/a
40	E2F4	chr1:155733305-155733505	MCF10A-Er-Src	breast:	n/a	n/a
41	EP300	chr1:155733176-155733637	A549	lung:	n/a	chr1:155733488-155733502
42	FOS	chr1:155733135-155733771	MCF10A-Er-Src	breast:	n/a	chr1:155733303-155733314
43	FOS	chr1:155733147-155733645	MCF10A-Er-Src	breast:	n/a	chr1:155733303-155733314
44	FOS	chr1:155733134-155733694	MCF10A-Er-Src	breast:	n/a	chr1:155733303-155733314
45	FOS	chr1:155733135-155733676	MCF10A-Er-Src	breast:	n/a	chr1:155733303-155733314
46	FOS	chr1:155733135-155733507	HUVEC	blood vessel:	n/a	chr1:155733303-155733314
47	FOSL1	chr1:155733206-155733442	HCT-116	colon:	n/a	n/a
48	FOSL1	chr1:155733226-155733428	HCT-116	colon:	n/a	n/a
49	FOSL2	chr1:155733131-155733617	A549	lung:	n/a	n/a
50	FOSL2	chr1:155733208-155733540	SK-N-SH	brain:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr1:155723093..155728376-chr1:155729603..155732543,6	K562	blood:
2	chr1:155722602..155725038-chr1:155735095..155737903,2	K562	blood:
3	chr1:155733230..155735390-chr1:155735568..155737501,2	K562	blood:
4	chr1:155730706..155733174-chr1:155733951..155736426,2	K562	blood:
5	chr1:155733230..155735390-chr1:155735568..155738519,3	K562	blood:
6	chr1:155733230..155735390-chr1:155735568..155738519,3	K562	blood:
7	chr1:155730706..155733174-chr1:155733951..155736426,2	K562	blood:
8	chr1:155618049..155618574-chr1:155733303..155733817,4	MCF-7	breast:
9	chr1:155733230..155735390-chr1:155735568..155737501,2	K562	blood:
10	chr1:155729870..155731926-chr1:155731964..155733488,2	MCF-7	breast:

No data

Variant related genes	Relation type
GON4L	TF binding region
ENSG00000116580	chromatin interactions

Extended variants
information (count: 258 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:258 , 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	rs111667027	chr1:155732270-155732271	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs141513443	chr1:155732304-155732305	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs554902355	chr1:155732321-155732322	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs146191124	chr1:155732328-155732329	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs540548574	chr1:155732365-155732366	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs528816287	chr1:155732379-155732380	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs576837207	chr1:155732407-155732408	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs544154144	chr1:155732432-155732433	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs111282231	chr1:155732456-155732457	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34168093	chr1:155732494-155732495	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs189707171	chr1:155732509-155732510	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs202175150	chr1:155732527-155732528	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs149894251	chr1:155732542-155732543	Strong transcription Weak transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs560946285	chr1:155732621-155732622	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs528260079	chr1:155732623-155732624	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184124461	chr1:155732676-155732677	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113516516	chr1:155732682-155732683	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148657390	chr1:155732691-155732692	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560205409	chr1:155732744-155732745	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs568822289	chr1:155732749-155732750	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs535994117	chr1:155732758-155732759	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs554623884	chr1:155732759-155732760	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573119077	chr1:155732770-155732771	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs534087147	chr1:155732781-155732782	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs558828972	chr1:155732783-155732784	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577165369	chr1:155732784-155732785	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs188579297	chr1:155732804-155732805	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542197361	chr1:155732806-155732807	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574747337	chr1:155732821-155732822	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541973226	chr1:155732852-155732853	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562185093	chr1:155732888-155732889	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs560528813	chr1:155732945-155732946	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191898082	chr1:155732947-155732948	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540478344	chr1:155732954-155732955	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs565062143	chr1:155732978-155732979	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs532480331	chr1:155733000-155733001	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
37	rs376244952	chr1:155733045-155733046	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
38	rs183389209	chr1:155733072-155733073	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
39	rs187182570	chr1:155733119-155733120	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
40	rs373018393	chr1:155733134-155733135	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
41	rs369733634	chr1:155733158-155733159	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
42	rs529659780	chr1:155733161-155733162	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
43	rs369208847	chr1:155733194-155733195	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	n/a	n/a	Overlapped CNVs	n/a
44	rs607790	chr1:155733214-155733215	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs201126347	chr1:155733237-155733238	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs373768203	chr1:155733248-155733249	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs607834	chr1:155733257-155733258	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs367656870	chr1:155733315-155733316	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs566184057	chr1:155733317-155733318	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs72706143	chr1:155733358-155733359	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:100)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Dihydropyrimidine dehydrogenase deficiency	18421352	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155715400-155739200	Weak transcription	Fetal Heart	heart
2	chr1:155715400-155789200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr1:155715600-155764600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr1:155716000-155793400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:155716600-155781800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:155717200-155761000	Strong transcription	Fetal Stomach	stomach
7	chr1:155717400-155733400	Strong transcription	Brain Anterior Caudate	brain
8	chr1:155717400-155795800	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr1:155717600-155733800	Strong transcription	Spleen	Spleen
10	chr1:155717600-155750200	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr1:155720200-155732800	Strong transcription	Monocytes-CD14+_RO01746	blood
12	chr1:155720200-155732800	Strong transcription	Osteobl	bone
13	chr1:155720200-155733000	Strong transcription	Primary monocytes fromperipheralblood	blood
14	chr1:155720200-155733800	Strong transcription	Sigmoid Colon	Sigmoid Colon
15	chr1:155720200-155745400	Strong transcription	Fetal Muscle Leg	muscle
16	chr1:155720200-155748600	Strong transcription	HUES48 Cell Line	embryonic stem cell
17	chr1:155720200-155748800	Strong transcription	Duodenum Mucosa	Duodenum
18	chr1:155720200-155748800	Strong transcription	Rectal Mucosa Donor 29	rectum
19	chr1:155720200-155749000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
20	chr1:155720200-155749600	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
21	chr1:155720200-155750200	Strong transcription	Primary T cells from cord blood	blood
22	chr1:155720200-155750600	Strong transcription	Primary hematopoietic stem cells short term culture	blood
23	chr1:155720200-155755800	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr1:155720200-155756200	Strong transcription	Primary T helper cells fromperipheralblood	blood
25	chr1:155720200-155756600	Strong transcription	HUES6 Cell Line	embryonic stem cell
26	chr1:155720200-155798200	Strong transcription	Fetal Thymus	thymus
27	chr1:155720200-155803600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr1:155720400-155732600	Strong transcription	HSMM	muscle
29	chr1:155720400-155732800	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr1:155720400-155732800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr1:155720400-155733000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr1:155720400-155733000	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr1:155720400-155733800	Strong transcription	Left Ventricle	heart
34	chr1:155720400-155743200	Strong transcription	Stomach Smooth Muscle	stomach
35	chr1:155720400-155743200	Strong transcription	Thymus	Thymus
36	chr1:155720400-155750200	Strong transcription	Adipose Nuclei	Adipose
37	chr1:155720400-155750400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr1:155720400-155750600	Strong transcription	Dnd41	blood
39	chr1:155720400-155755600	Strong transcription	Placenta	Placenta
40	chr1:155720400-155756400	Strong transcription	Liver	Liver
41	chr1:155720400-155760800	Strong transcription	Primary T cells fromperipheralblood	blood
42	chr1:155720400-155796800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr1:155720600-155732800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr1:155720600-155733400	Strong transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr1:155720600-155733400	Strong transcription	Brain Germinal Matrix	brain
46	chr1:155720600-155733400	Strong transcription	Rectal Mucosa Donor 31	rectum
47	chr1:155720600-155733600	Strong transcription	Skeletal Muscle Male	skeletal muscle
48	chr1:155720600-155733800	Strong transcription	Fetal Lung	lung
49	chr1:155720600-155735800	Strong transcription	Rectal Smooth Muscle	rectum
50	chr1:155720600-155743200	Strong transcription	Fetal Brain Female	brain

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