Variant report

Variant	esv1818312
Chromosome Location	chr5:60169859-60200993
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:227)
CpG islands
(count:122)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:227 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:60181991-60182269	HepG2	liver:	n/a	n/a
2	ARID3A	chr5:60179163-60179195	K562	blood:	n/a	n/a
3	CEBPB	chr5:60189614-60189869	HepG2	liver:	n/a	chr5:60189735-60189746 chr5:60189694-60189705
4	CHD1	chr5:60187619-60187641	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr5:60178988-60179441	MCF-7	breast:	n/a	n/a
6	CTCF	chr5:60179160-60179310	Hela-S3	cervix:	n/a	n/a
7	CTCF	chr5:60179160-60179310	NB4	blood:	n/a	n/a
8	CTCF	chr5:60179120-60179270	WI-38	lung:	n/a	n/a
9	CTCF	chr5:60179139-60179344	HepG2	liver:	n/a	n/a
10	CTCF	chr5:60179180-60179330	MCF-7	breast:	n/a	n/a
11	CTCF	chr5:60179180-60179330	AG09319	gingival:	n/a	n/a
12	CTCF	chr5:60179140-60179290	SAEC	small airway:	n/a	n/a
13	CTCF	chr5:60179520-60179670	HCT-116	colon:	n/a	n/a
14	CTCF	chr5:60178983-60179529	HCT-116	colon:	n/a	n/a
15	CTCF	chr5:60179260-60179410	HA-sp	spinal cord:	n/a	n/a
16	CTCF	chr5:60179220-60179370	GM12868	blood:	n/a	n/a
17	CTCF	chr5:60179180-60179330	HCM	heart:	n/a	n/a
18	CTCF	chr5:60179240-60179390	BE2_C	brain:	n/a	n/a
19	CTCF	chr5:60179140-60179290	WERI-Rb-1	eye:	n/a	n/a
20	CTCF	chr5:60179140-60179290	K562	blood:	n/a	n/a
21	CTCF	chr5:60179096-60179420	MCF-7	breast:	n/a	n/a
22	CTCF	chr5:60179047-60179371	A549	lung:	n/a	n/a
23	CTCF	chr5:60179212-60179272	MCF-7	breast:	n/a	n/a
24	CTCF	chr5:60179180-60179330	GM06990	blood:	n/a	n/a
25	CTCF	chr5:60179040-60179190	A549	lung:	n/a	n/a
26	CTCF	chr5:60179100-60179250	GM12878	blood:	n/a	n/a
27	CTCF	chr5:60179160-60179310	GM12872	blood:	n/a	n/a
28	CTCF	chr5:60179180-60179330	AG04450	lung:	n/a	n/a
29	CTCF	chr5:60179172-60179274	MCF-7	breast:	n/a	n/a
30	CTCF	chr5:60179180-60179330	HMF	breast:	n/a	n/a
31	CTCF	chr5:60179095-60179373	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr5:60179120-60179270	WERI-Rb-1	eye:	n/a	n/a
33	CTCF	chr5:60179146-60179358	GM13977	blood:	n/a	n/a
34	CTCF	chr5:60179180-60179330	GM12801	blood:	n/a	n/a
35	CTCF	chr5:60179200-60179350	GM12875	blood:	n/a	n/a
36	CTCF	chr5:60179120-60179270	GM12874	blood:	n/a	n/a
37	CTCF	chr5:60179200-60179350	GM12869	blood:	n/a	n/a
38	CTCF	chr5:60179200-60179350	HCT-116	colon:	n/a	n/a
39	CTCF	chr5:60179160-60179310	HPAF	blood vessel:	n/a	n/a
40	CTCF	chr5:60179207-60179269	Spleen_OC	spleen:	n/a	n/a
41	CTCF	chr5:60179060-60179210	HAc	cerebellar:	n/a	n/a
42	CTCF	chr5:60179160-60179310	AG10803	skin:	n/a	n/a
43	CTCF	chr5:60179120-60179270	AG10803	skin:	n/a	n/a
44	CTCF	chr5:60179160-60179310	GM12874	blood:	n/a	n/a
45	CTCF	chr5:60179120-60179270	HepG2	liver:	n/a	n/a
46	CTCF	chr5:60179071-60179417	K562	blood:	n/a	n/a
47	CTCF	chr5:60179200-60179350	NHEK	skin:	n/a	n/a
48	CTCF	chr5:60179160-60179310	AG09319	gingival:	n/a	n/a
49	CTCF	chr5:60179200-60179350	HRE	kidney:	n/a	n/a
50	CTCF	chr5:60179120-60179379	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:60187211-60187261	SK-N-SH_RA	brain:	n/a
2	chr5:60170058-60170108	HAEpiC	amniotic membrane:	n/a
3	chr5:60170058-60170108	HUVEC	blood vessel:	n/a
4	chr5:60170058-60170108	GM12878	blood:	n/a
5	chr5:60187211-60187261	HRE	kidney:	n/a
6	chr5:60170058-60170108	GM12892	blood:	n/a
7	chr5:60187211-60187261	A549	lung:	n/a
8	chr5:60170058-60170108	PANC-1	pancreas:	n/a
9	chr5:60170058-60170108	HRE	kidney:	n/a
10	chr5:60187211-60187261	GM19239	blood:	n/a
11	chr5:60187211-60187261	Hela-S3	cervix:	n/a
12	chr5:60170058-60170108	BE2_C	brain:	n/a
13	chr5:60170058-60170108	HPAEpiC	pulmonary alveolar:	n/a
14	chr5:60187211-60187261	ovcar-3	ovarian:	n/a
15	chr5:60170058-60170108	GM06990	blood:	n/a
16	chr5:60170058-60170108	NHDF-neo	bronchial:	n/a
17	chr5:60170058-60170108	SAEC	small airway:	n/a
18	chr5:60170058-60170108	HRCEpiC	kidney:	n/a
19	chr5:60170058-60170108	NB4	blood:	n/a
20	chr5:60187211-60187261	AG04449	skin:	fetal
21	chr5:60187211-60187261	GM12892	blood:	n/a
22	chr5:60170058-60170108	AG09319	gingival:	n/a
23	chr5:60187211-60187261	IMR90	lung:	fetal
24	chr5:60170058-60170108	HCM	heart:	n/a
25	chr5:60187211-60187261	HPAEpiC	pulmonary alveolar:	n/a
26	chr5:60170058-60170108	GM12891	blood:	n/a
27	chr5:60170058-60170108	ProgFib	skin:	n/a
28	chr5:60170058-60170108	AoSMC	blood vessel:	n/a
29	chr5:60187211-60187261	HCM	heart:	n/a
30	chr5:60187211-60187261	SK-N-MC	brain:	n/a
31	chr5:60170058-60170108	HRPEpiC	eye:	n/a
32	chr5:60170058-60170108	CMK	blood:	n/a
33	chr5:60187211-60187261	MCF-7	breast:	n/a
34	chr5:60187211-60187261	NHBE	bronchial:	n/a
35	chr5:60170058-60170108	BJ	skin:	n/a
36	chr5:60170058-60170108	HCPEpiC	choroid plexus:	n/a
37	chr5:60187211-60187261	HRCEpiC	kidney:	n/a
38	chr5:60187211-60187261	GM06990	blood:	n/a
39	chr5:60187211-60187261	SK-N-SH	brain:	n/a
40	chr5:60187211-60187261	GM12891	blood:	n/a
41	chr5:60187211-60187261	HL-60	blood:	n/a
42	chr5:60170058-60170108	SKMC	muscle:	n/a
43	chr5:60187211-60187261	T-47D	breast:	n/a
44	chr5:60187211-60187261	HCT-116	colon:	n/a
45	chr5:60170058-60170108	PFSK-1	brain:	n/a
46	chr5:60187211-60187261	U87	brain:	n/a
47	chr5:60170058-60170108	MCF-7	breast:	n/a
48	chr5:60187211-60187261	HEEpiC	esophagus:	n/a
49	chr5:60187211-60187261	NB4	blood:	n/a
50	chr5:60170058-60170108	Hela-S3	cervix:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
2	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:
3	chr5:60180292..60182864-chr5:60197652..60199480,2	MCF-7	breast:
4	chr5:60199382..60201400-chr5:60201974..60203709,2	MCF-7	breast:
5	chr5:60182235..60184103-chr5:60240425..60242925,2	MCF-7	breast:
6	chr5:60199648..60201758-chr5:60214066..60215878,2	K562	blood:
7	chr5:60198217..60200090-chr5:60210725..60213432,2	K562	blood:
8	chr5:59973507..59975333-chr5:60177921..60180223,2	MCF-7	breast:
9	chr5:60197378..60199717-chr5:60210725..60212735,2	K562	blood:
10	chr5:60168971..60171964-chr5:60184118..60186790,2	K562	blood:

No data

Variant related genes	Relation type
GNL3LP1	TF binding region
GNL3LP1	CpG island
ENSG00000049167	chromatin interactions
ENSG00000233847	chromatin interactions
ENSG00000164182	chromatin interactions

Extended variants
information (count: 1314 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1314 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4647158	chr5:60169859-60169860	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs4647157	chr5:60169923-60169924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs4647156	chr5:60169984-60169985	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs4647155	chr5:60170003-60170004	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs559175991	chr5:60170031-60170032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565773632	chr5:60170038-60170039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs145230004	chr5:60170106-60170107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs4647154	chr5:60170146-60170147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs1047032	chr5:60170161-60170162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs568206790	chr5:60170165-60170166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373740060	chr5:60170177-60170178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs537108408	chr5:60170179-60170180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs147992873	chr5:60170188-60170189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs577134348	chr5:60170195-60170196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4647153	chr5:60170205-60170206	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs112808360	chr5:60170252-60170253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs567684336	chr5:60170329-60170330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs3117	chr5:60170337-60170338	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs368665460	chr5:60170392-60170393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs4647152	chr5:60170406-60170407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562220187	chr5:60170426-60170427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377745901	chr5:60170435-60170436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574585335	chr5:60170456-60170457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374154824	chr5:60170463-60170464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143147836	chr5:60170472-60170473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs368676801	chr5:60170474-60170475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543517781	chr5:60170484-60170485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs138752036	chr5:60170493-60170494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs41562418	chr5:60170542-60170543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4647151	chr5:60170558-60170559	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs186565039	chr5:60170583-60170584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4647150	chr5:60170605-60170606	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs528311994	chr5:60170621-60170622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190080881	chr5:60170628-60170629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs567869945	chr5:60170676-60170677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530925582	chr5:60170677-60170678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558904437	chr5:60170683-60170684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs542202272	chr5:60170704-60170705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561998652	chr5:60170737-60170738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4647149	chr5:60170834-60170835	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs4647148	chr5:60170842-60170843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs182646370	chr5:60170894-60170895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539817407	chr5:60170960-60170961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs4647147	chr5:60170977-60170978	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs567160110	chr5:60171004-60171005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536106967	chr5:60171015-60171016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs185423188	chr5:60171021-60171022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs150260438	chr5:60171057-60171058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543578855	chr5:60171063-60171064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556999935	chr5:60171070-60171071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Colorectal cancer	21645411	CNVD
Gastric cancer	22152101	CNVD
Oesophago-gastric ulcer	22152101	CNVD
Ovarian cancer	21781307	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
DNA damage stimulus	22844521	CNVD
DNA repair	22844521	CNVD
Breast cancer	21785460	CNVD
Spinal muscular atrophy	22422766	CNVD
Spinal muscular atrophy	22558076	CNVD
Spinal muscular atrophy	21320981	CNVD
Spinal muscular atrophy	21762474	CNVD
Cancer	16751803	CNVD
Autism	22495311	CNVD
Intellectual disability	22102821	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	22032731	CNVD
Prostate cancer	21965145	CNVD
Esophageal cancer	20955586	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
adenomatous polyposis	22470819	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Hepatocellular carcinoma	16750200	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Bladder cancer	21909424	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17133270	CNVD
Breast cancer	19602461	CNVD
Renal cell carcinoma	18194544	CNVD
abnormal development	18461090	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Neuroticism	17667963	CNVD
Contiguous gene syndrome	19525295	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:60166600-60177000	Weak transcription	Ovary	ovary
2	chr5:60167200-60192600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr5:60167400-60186000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr5:60167800-60182000	Weak transcription	Left Ventricle	heart
5	chr5:60167800-60187800	Weak transcription	Primary T cells from cord blood	blood
6	chr5:60167800-60188400	Weak transcription	Liver	Liver
7	chr5:60167800-60192800	Weak transcription	Primary hematopoietic stem cells	blood
8	chr5:60167800-60228200	Weak transcription	Psoas Muscle	Psoas
9	chr5:60168400-60191000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr5:60169000-60185800	Weak transcription	Adipose Nuclei	Adipose
11	chr5:60169800-60191000	Weak transcription	NH-A	brain
12	chr5:60175200-60188400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr5:60175200-60188400	Weak transcription	Right Ventricle	heart
14	chr5:60175400-60177000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr5:60175400-60177000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:60175400-60177000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr5:60175800-60188200	Weak transcription	Gastric	stomach
18	chr5:60175800-60188200	Weak transcription	Stomach Smooth Muscle	stomach
19	chr5:60175800-60239400	Weak transcription	NHEK	skin
20	chr5:60176400-60220400	Weak transcription	Esophagus	oesophagus
21	chr5:60176600-60176800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr5:60176600-60178000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
23	chr5:60176600-60178200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr5:60176600-60179600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
25	chr5:60176600-60188000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr5:60176800-60177200	ZNF genes & repeats	Fetal Lung	lung
27	chr5:60176800-60178000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr5:60176800-60180000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr5:60176800-60188200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr5:60177000-60177200	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr5:60177000-60177400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr5:60177000-60177400	ZNF genes & repeats	Ovary	ovary
33	chr5:60177000-60178000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr5:60177000-60178400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr5:60177000-60178600	ZNF genes & repeats	Fetal Intestine Small	intestine
36	chr5:60177000-60178600	ZNF genes & repeats	Fetal Stomach	stomach
37	chr5:60177000-60190400	Weak transcription	HSMM	muscle
38	chr5:60177200-60178400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr5:60177200-60179200	Weak transcription	Fetal Lung	lung
40	chr5:60177200-60188800	Weak transcription	Monocytes-CD14+_RO01746	blood
41	chr5:60177200-60189800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
42	chr5:60177200-60239600	Weak transcription	HSMMtube	muscle
43	chr5:60177400-60178000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr5:60177400-60180800	Weak transcription	Ovary	ovary
45	chr5:60177400-60188200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr5:60177400-60188600	Weak transcription	A549	lung
47	chr5:60177400-60188800	Weak transcription	Primary B cells from cord blood	blood
48	chr5:60177400-60188800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr5:60177400-60192600	Weak transcription	Primary T cells fromperipheralblood	blood
50	chr5:60177400-60232800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung

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