Variant report

Variant	esv2762194
Chromosome Location	chr1:155063145-155067283
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:48)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:48 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:155064094..155065891-chr1:155117626..155119134,2	MCF-7	breast:
2	chr1:155065499..155067791-chr1:155070241..155073223,2	MCF-7	breast:
3	chr1:155057731..155060125-chr1:155060482..155063355,3	K562	blood:
4	chr1:155056065..155060440-chr1:155062354..155065779,6	K562	blood:
5	chr1:155063203..155065869-chr1:155133125..155134696,2	K562	blood:
6	chr1:155063776..155066689-chr1:155134444..155136393,2	MCF-7	breast:
7	chr1:155062500..155064343-chr1:155162863..155164814,2	K562	blood:
8	chr1:155066673..155067248-chr1:155141597..155142397,2	MCF-7	breast:
9	chr1:155063197..155065569-chr1:155078354..155080513,2	K562	blood:
10	chr1:155066781..155067437-chr1:155099017..155099580,2	MCF-7	breast:
11	chr1:155063588..155065472-chr1:155139784..155141178,19	K562	blood:
12	chr1:155066619..155069585-chr1:155195780..155198713,2	K562	blood:
13	chr1:155066558..155067106-chr1:155140003..155140931,3	K562	blood:
14	chr1:155065702..155067995-chr1:155139570..155140962,16	MCF-7	breast:
15	chr1:155063799..155064604-chr1:155100192..155100908,2	MCF-7	breast:
16	chr1:155066706..155067679-chr1:155149226..155149765,2	MCF-7	breast:
17	chr1:155064464..155066465-chr1:155098268..155100764,3	K562	blood:
18	chr1:155066341..155068339-chr1:155131182..155134101,2	MCF-7	breast:
19	chr1:155062424..155064059-chr1:155147918..155149990,2	K562	blood:
20	chr1:155066514..155068580-chr1:155068788..155070553,2	MCF-7	breast:
21	chr1:155063515..155065067-chr1:155139525..155141192,27	MCF-7	breast:
22	chr1:155049589..155073019-chr1:155085330..155115362,149	MCF-7	breast:
23	chr1:155062448..155069217-chr1:155142816..155147773,12	MCF-7	breast:
24	chr1:155066957..155067711-chr1:155138966..155139492,2	MCF-7	breast:
25	chr1:155062611..155066935-chr1:155144495..155147775,5	MCF-7	breast:
26	chr1:155063703..155067297-chr1:155143302..155147272,4	K562	blood:
27	chr1:155059639..155063596-chr1:155149285..155151101,3	MCF-7	breast:
28	chr1:155036626..155039573-chr1:155062650..155065078,2	K562	blood:
29	chr1:154990145..154990649-chr1:155063543..155064116,2	K562	blood:
30	chr1:155066527..155067288-chr1:155106043..155106834,2	MCF-7	breast:
31	chr1:155055416..155060440-chr1:155063419..155068026,8	K562	blood:
32	chr1:155061833..155068204-chr1:155135824..155142287,19	MCF-7	breast:
33	chr1:155064469..155067923-chr1:155161991..155164572,4	MCF-7	breast:
34	chr1:155061878..155067935-chr1:155138836..155144212,15	MCF-7	breast:
35	chr1:155063589..155064900-chr1:155139461..155140960,10	MCF-7	breast:
36	chr1:155066076..155068136-chr1:155139564..155141486,24	MCF-7	breast:
37	chr1:154931783..154934509-chr1:155065563..155068170,2	MCF-7	breast:
38	chr1:154913750..154914351-chr1:155063298..155064132,2	MCF-7	breast:
39	chr1:155051153..155052949-chr1:155062882..155065353,2	K562	blood:
40	chr1:155063960..155065905-chr1:155106879..155109737,2	K562	blood:
41	chr1:155064648..155066932-chr1:155147928..155150182,2	K562	blood:
42	chr1:155066425..155068289-chr1:155084131..155086403,2	MCF-7	breast:
43	chr1:155034616..155035354-chr1:155064122..155064830,2	K562	blood:
44	chr1:155061300..155064000-chr1:155163314..155166303,2	K562	blood:
45	chr1:155063649..155064298-chr1:155097109..155097861,2	MCF-7	breast:
46	chr1:155056491..155066482-chr1:155136760..155147519,21	K562	blood:
47	chr1:155067274..155067813-chr1:155140046..155140799,2	K562	blood:
48	chr1:155064687..155066465-chr1:155098268..155100764,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000179085	chromatin interactions
ENSG00000271380	chromatin interactions
ENSG00000271748	chromatin interactions
ENSG00000185499	chromatin interactions
ENSG00000163348	chromatin interactions
ENSG00000202027	chromatin interactions
ENSG00000143537	chromatin interactions
ENSG00000169241	chromatin interactions
ENSG00000160766	chromatin interactions
ENSG00000169231	chromatin interactions
ENSG00000169242	chromatin interactions
ENSG00000163462	chromatin interactions
ENSG00000143590	chromatin interactions
ENSG00000163463	chromatin interactions

Extended variants
information (count: 133 )
Associated
traits (count: 109 )

Variant overlapped rSNPs/rCNVs (count:133 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376884588	chr1:155063207-155063208	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
2	rs559801013	chr1:155063210-155063211	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
3	rs148113725	chr1:155063240-155063241	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
4	rs551795056	chr1:155063244-155063245	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
5	rs371277548	chr1:155063246-155063247	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
6	rs531262187	chr1:155063304-155063305	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
7	rs186495675	chr1:155063337-155063338	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
8	rs141942581	chr1:155063371-155063372	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
9	rs375360766	chr1:155063377-155063378	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
10	rs150677096	chr1:155063391-155063392	Weak transcription Enhancers	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
11	rs374594189	chr1:155063405-155063406	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
12	rs191382535	chr1:155063409-155063410	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
13	rs113057340	chr1:155063413-155063414	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs565775862	chr1:155063458-155063459	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs373997476	chr1:155063554-155063555	Weak transcription Enhancers Bivalent Enhancer Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs539148985	chr1:155063635-155063636	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs557377289	chr1:155063643-155063644	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs376017418	chr1:155063680-155063681	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs549643156	chr1:155063755-155063756	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs543346346	chr1:155063784-155063785	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs555263900	chr1:155063796-155063797	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs370021515	chr1:155063813-155063814	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs569820709	chr1:155063926-155063927	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs541232512	chr1:155063930-155063931	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs180872761	chr1:155063961-155063962	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs578085613	chr1:155063996-155063997	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Weak transcription	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs142274118	chr1:155064094-155064095	Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
28	rs563710921	chr1:155064145-155064146	Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs146399535	chr1:155064149-155064150	Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs549367020	chr1:155064158-155064159	Bivalent Enhancer Enhancers Active TSS Genic enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs139058440	chr1:155064248-155064249	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs528737313	chr1:155064299-155064300	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs202208864	chr1:155064319-155064320	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs547210965	chr1:155064344-155064345	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs571744376	chr1:155064374-155064375	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
36	rs539547799	chr1:155064382-155064383	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
37	rs368502058	chr1:155064390-155064391	Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
38	rs551045582	chr1:155064460-155064461	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
39	rs373523529	chr1:155064505-155064506	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
40	rs184920110	chr1:155064507-155064508	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
41	rs374693884	chr1:155064561-155064562	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
42	rs536652385	chr1:155064570-155064571	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
43	rs562077254	chr1:155064582-155064583	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs371574291	chr1:155064584-155064585	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs554903058	chr1:155064590-155064591	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs573919634	chr1:155064615-155064616	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs534611749	chr1:155064645-155064646	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs553163442	chr1:155064686-155064687	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs190960368	chr1:155064690-155064691	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs545192171	chr1:155064708-155064709	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS	Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:109)

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	20409316	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
Chronic lymphocytic leukemia	22228453	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
Aortic dissecting aneurysms	22263138	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:155058400-155063800	Weak transcription	HSMM	muscle
2	chr1:155058600-155063800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr1:155058600-155063800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr1:155058600-155063800	Weak transcription	HUVEC	blood vessel
5	chr1:155058600-155066000	Weak transcription	Right Atrium	heart
6	chr1:155059000-155063400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
7	chr1:155059000-155063600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr1:155059000-155063600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr1:155059000-155063600	Weak transcription	H9 Cell Line	embryonic stem cell
10	chr1:155059000-155063600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr1:155059000-155063600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr1:155059000-155063600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr1:155059000-155063600	Weak transcription	Liver	Liver
14	chr1:155059000-155063600	Weak transcription	Brain Anterior Caudate	brain
15	chr1:155059000-155063600	Weak transcription	Brain Cingulate Gyrus	brain
16	chr1:155059000-155063600	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr1:155059000-155063600	Weak transcription	Brain Substantia Nigra	brain
18	chr1:155059000-155063600	Weak transcription	Colon Smooth Muscle	Colon
19	chr1:155059000-155063600	Weak transcription	Duodenum Mucosa	Duodenum
20	chr1:155059000-155063600	Weak transcription	Pancreas	Pancrea
21	chr1:155059000-155063600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr1:155059000-155063600	Weak transcription	Skeletal Muscle Male	skeletal muscle
23	chr1:155059000-155063600	Weak transcription	Stomach Mucosa	stomach
24	chr1:155059000-155063600	Weak transcription	NHEK	skin
25	chr1:155059000-155063800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr1:155059000-155063800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr1:155059000-155063800	Weak transcription	Brain Angular Gyrus	brain
28	chr1:155059000-155063800	Weak transcription	Fetal Brain Female	brain
29	chr1:155059000-155063800	Weak transcription	Gastric	stomach
30	chr1:155059000-155063800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr1:155059000-155063800	Weak transcription	GM12878-XiMat	blood
32	chr1:155059000-155064200	Weak transcription	Left Ventricle	heart
33	chr1:155059000-155066200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr1:155059200-155063600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
35	chr1:155059200-155063600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr1:155059200-155063600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
37	chr1:155059200-155063600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr1:155059200-155063600	Weak transcription	Brain Hippocampus Middle	brain
39	chr1:155059200-155063600	Weak transcription	Colonic Mucosa	Colon
40	chr1:155059200-155063600	Weak transcription	Rectal Smooth Muscle	rectum
41	chr1:155059200-155063600	Weak transcription	Right Ventricle	heart
42	chr1:155059200-155063600	Weak transcription	Sigmoid Colon	Sigmoid Colon
43	chr1:155059200-155063600	Weak transcription	HMEC	breast
44	chr1:155059200-155063800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
45	chr1:155059200-155063800	Weak transcription	Primary T helper cells fromperipheralblood	blood
46	chr1:155059200-155063800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
47	chr1:155059200-155063800	Weak transcription	Adipose Nuclei	Adipose
48	chr1:155059200-155063800	Weak transcription	Fetal Thymus	thymus
49	chr1:155059200-155063800	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr1:155059200-155066600	Weak transcription	Primary B cells from cord blood	blood

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