Variant report

Variant	esv1850212
Chromosome Location	chr17:67081732-67117428
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:426)
CpG islands
(count:0)
Chromatin interactive
region (count:36)
LncRNA
region (count:5)
Mature miRNA
region (count: 4)
miRNA target
sites (count:0)

(count:426 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:67095884-67095906	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:67099561-67100456	K562	blood:	n/a	n/a
3	ARID3A	chr17:67089305-67090018	K562	blood:	n/a	n/a
4	ATF1	chr17:67089408-67089787	K562	blood:	n/a	n/a
5	ATF1	chr17:67099614-67100149	K562	blood:	n/a	n/a
6	ATF2	chr17:67113978-67114838	GM12878	blood:	n/a	n/a
7	ATF2	chr17:67113943-67114388	GM12878	blood:	n/a	n/a
8	ATF2	chr17:67111814-67112633	GM12878	blood:	n/a	n/a
9	ATF2	chr17:67111910-67112667	GM12878	blood:	n/a	n/a
10	ATF3	chr17:67099819-67100032	K562	blood:	n/a	chr17:67099847-67099860 chr17:67099849-67099860
11	ATF3	chr17:67089445-67089791	K562	blood:	n/a	n/a
12	BACH1	chr17:67089457-67089837	K562	blood:	n/a	n/a
13	BATF	chr17:67112080-67112476	GM12878	blood:	n/a	n/a
14	BATF	chr17:67114297-67114715	GM12878	blood:	n/a	chr17:67114471-67114482
15	BATF	chr17:67114039-67114253	GM12878	blood:	n/a	n/a
16	BATF	chr17:67114014-67114483	GM12878	blood:	n/a	chr17:67114471-67114482
17	BCL11A	chr17:67111962-67112539	GM12878	blood:	n/a	n/a
18	BCL11A	chr17:67114028-67114297	GM12878	blood:	n/a	chr17:67114134-67114143
19	BCL11A	chr17:67112124-67112482	GM12878	blood:	n/a	n/a
20	BCL3	chr17:67111932-67112561	GM12878	blood:	n/a	n/a
21	BCLAF1	chr17:67111963-67112617	GM12878	blood:	n/a	n/a
22	BHLHE40	chr17:67113981-67114829	GM12878	blood:	n/a	n/a
23	BHLHE40	chr17:67112037-67112924	GM12878	blood:	n/a	n/a
24	BHLHE40	chr17:67089168-67089845	K562	blood:	n/a	n/a
25	BHLHE40	chr17:67103603-67103615	GM12878	blood:	n/a	n/a
26	BHLHE40	chr17:67099598-67100263	K562	blood:	n/a	n/a
27	BHLHE40	chr17:67086647-67086829	K562	blood:	n/a	n/a
28	BHLHE40	chr17:67084981-67085086	K562	blood:	n/a	n/a
29	BRCA1	chr17:67088556-67088568	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr17:67089320-67089889	K562	blood:	n/a	n/a
31	CBX3	chr17:67084988-67085319	K562	blood:	n/a	n/a
32	CBX3	chr17:67084746-67085330	K562	blood:	n/a	n/a
33	CBX3	chr17:67089386-67089826	K562	blood:	n/a	n/a
34	CBX3	chr17:67099607-67100349	K562	blood:	n/a	n/a
35	CCNT2	chr17:67099638-67100538	K562	blood:	n/a	chr17:67099962-67099982
36	CCNT2	chr17:67089287-67089821	K562	blood:	n/a	n/a
37	CEBPB	chr17:67116181-67116337	K562	blood:	n/a	n/a
38	CEBPB	chr17:67111913-67112706	GM12878	blood:	n/a	n/a
39	CEBPB	chr17:67099697-67100406	K562	blood:	n/a	n/a
40	CEBPB	chr17:67105655-67105950	HepG2	liver:	n/a	chr17:67105796-67105807
41	CEBPB	chr17:67089301-67089850	K562	blood:	n/a	n/a
42	CEBPB	chr17:67111908-67111958	K562	blood:	n/a	n/a
43	CEBPB	chr17:67094938-67095113	HepG2	liver:	n/a	chr17:67095008-67095019
44	CEBPB	chr17:67099763-67100159	K562	blood:	n/a	n/a
45	CEBPB	chr17:67099906-67100028	K562	blood:	n/a	n/a
46	CEBPB	chr17:67102609-67102801	K562	blood:	n/a	n/a
47	CEBPB	chr17:67089382-67089829	K562	blood:	n/a	n/a
48	CEBPB	chr17:67094967-67095034	K562	blood:	n/a	chr17:67095008-67095019
49	CEBPB	chr17:67115803-67116037	HepG2	liver:	n/a	n/a
50	CEBPB	chr17:67094933-67095132	H1-hESC	embryonic stem cell:	n/a	chr17:67095008-67095019

No data

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:67087494..67092191-chr17:67094325..67097858,5	K562	blood:
2	chr17:67105618..67107692-chr17:67108283..67110713,2	K562	blood:
3	chr17:67100035..67103049-chr17:67106877..67108749,3	K562	blood:
4	chr17:67115823..67118302-chr17:67121333..67123082,2	K562	blood:
5	chr17:67100035..67103049-chr17:67106877..67108749,3	K562	blood:
6	chr17:67096035..67097886-chr17:67098176..67100772,2	K562	blood:
7	chr17:67083309..67086941-chr17:67087664..67091050,5	K562	blood:
8	chr17:67088212..67090645-chr17:67172453..67175365,2	K562	blood:
9	chr17:67087380..67090007-chr17:67103818..67105746,2	K562	blood:
10	chr17:67087380..67090007-chr17:67103818..67105746,2	K562	blood:
11	chr17:67072787..67074719-chr17:67087399..67089601,2	K562	blood:
12	chr17:67088137..67090811-chr17:67098460..67099975,2	K562	blood:
13	chr17:67101159..67103810-chr17:67103902..67105900,2	MCF-7	breast:
14	chr17:67103041..67104910-chr17:67106745..67108677,2	K562	blood:
15	chr17:67098233..67101602-chr17:67102782..67105641,3	K562	blood:
16	chr17:67108053..67109603-chr17:67109897..67112627,2	K562	blood:
17	chr17:67096035..67097886-chr17:67098176..67100772,2	K562	blood:
18	chr17:67085517..67087191-chr17:67098879..67100448,2	K562	blood:
19	chr17:67114400..67115990-chr17:67171534..67173172,2	K562	blood:
20	chr17:67099587..67101559-chr17:67104865..67106411,2	K562	blood:
21	chr17:67074921..67077077-chr17:67087340..67089647,2	K562	blood:
22	chr17:67088137..67090811-chr17:67098460..67099975,2	K562	blood:
23	chr17:67083309..67086380-chr17:67087124..67091050,4	K562	blood:
24	chr17:67043107..67046503-chr17:67087487..67090701,3	K562	blood:
25	chr17:67115279..67117551-chr17:67138552..67141546,2	K562	blood:
26	chr17:67098233..67101602-chr17:67102782..67105641,3	K562	blood:
27	chr17:67105618..67107692-chr17:67108283..67110713,2	K562	blood:
28	chr17:67101159..67103810-chr17:67103902..67105900,2	MCF-7	breast:
29	chr17:67087494..67092191-chr17:67094325..67097858,5	K562	blood:
30	chr17:67042180..67045074-chr17:67080026..67082668,2	K562	blood:
31	chr17:67085517..67087191-chr17:67098879..67100448,2	K562	blood:
32	chr17:67084611..67087550-chr17:67148578..67150089,2	K562	blood:
33	chr17:67099587..67101559-chr17:67104865..67106411,2	K562	blood:
34	chr17:67091911..67095488-chr17:67096351..67099862,4	K562	blood:
35	chr17:67112395..67115325-chr17:67117156..67120723,3	K562	blood:
36	chr17:67103041..67104910-chr17:67106745..67108677,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAP2K6-9	chr17:67104074-67104302	NONHSAT055567
2	lnc-MAP2K6-9	chr17:67104683-67105015	NONHSAT055568
3	lnc-MAP2K6-9	chr17:67104212-67104310	NONHSAT055568
4	lnc-ABCA9-2	chr17:67090430-67091640	NONHSAT055564
5	lnc-MAP2K6-9	chr17:67104683-67105014	NONHSAT055567

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4524b-5p	chr17:67095711-67095731	MIMAT0022255
hsa-miR-4524a-3p	chr17:67095711-67095732	MIMAT0019063
hsa-miR-4524a-5p	chr17:67095747-67095768	MIMAT0019062
hsa-miR-4524b-3p	chr17:67095748-67095767	MIMAT0022256

No data

Variant related genes	Relation type
MIR4524A	TF binding region
ENSG00000267361	TF binding region
ABCA6	TF binding region
ENSG00000154262	chromatin interactions
ENSG00000154263	chromatin interactions
ENSG00000265331	chromatin interactions
ENSG00000154258	chromatin interactions
ENSG00000267361	chromatin interactions

Extended variants
information (count: 1391 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:1391 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2302133	chr17:67081732-67081733	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs372828923	chr17:67081735-67081736	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs201781263	chr17:67081744-67081745	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs199825394	chr17:67081765-67081766	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200806055	chr17:67081768-67081769	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs267605021	chr17:67081771-67081772	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs561371331	chr17:67081774-67081775	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs145446871	chr17:67081787-67081788	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs377055785	chr17:67081811-67081812	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs2302134	chr17:67081830-67081831	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs141017176	chr17:67081837-67081838	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs199530183	chr17:67081900-67081901	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs565042800	chr17:67081924-67081925	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191770733	chr17:67081970-67081971	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs532923344	chr17:67081985-67081986	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551178643	chr17:67081996-67081997	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs78821320	chr17:67081997-67081998	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs34421831	chr17:67082021-67082022	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181839214	chr17:67082062-67082063	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548692784	chr17:67082073-67082074	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs567299110	chr17:67082084-67082085	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs538518911	chr17:67082091-67082092	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs186177746	chr17:67082144-67082145	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs556181553	chr17:67082161-67082162	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs557082835	chr17:67082179-67082180	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs550541512	chr17:67082225-67082226	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs12162136	chr17:67082266-67082267	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs150265875	chr17:67082291-67082292	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553113309	chr17:67082298-67082299	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs555656907	chr17:67082335-67082336	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116306615	chr17:67082367-67082368	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190083135	chr17:67082372-67082373	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372865781	chr17:67082376-67082377	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs576339208	chr17:67082398-67082399	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs543462300	chr17:67082438-67082439	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs74631971	chr17:67082442-67082443	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532492356	chr17:67082443-67082444	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs199804883	chr17:67082628-67082629	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs74001808	chr17:67082631-67082632	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72266060	chr17:67082638-67082639	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138436807	chr17:67082639-67082640	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs398031437	chr17:67082649-67082650	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs182691761	chr17:67082715-67082716	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559955580	chr17:67082763-67082764	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144845365	chr17:67082774-67082775	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138917560	chr17:67082787-67082788	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149559050	chr17:67082789-67082790	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144256500	chr17:67082799-67082800	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148324916	chr17:67082807-67082808	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs371602458	chr17:67082847-67082848	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Cancer	21129771	CNVD
Congenital generalized hypertrichosis terminalis	19463983	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Gingival hyperplasia	19463983	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neuroblastoma	20406844	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Breast cancer	21045282	CNVD
Epilepsy	22083797	CNVD
Sezary syndrome	18413736	CNVD
Honadal dysgenesis	21408189	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Basal cell lymphoma	17053054	CNVD
Acute monocytic leukemia	16498392	CNVD
Cancer	17440070	CNVD

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:67065600-67088600	Weak transcription	Pancreas	Pancrea
2	chr17:67067200-67099600	Weak transcription	Gastric	stomach
3	chr17:67067200-67111600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr17:67071800-67091400	Weak transcription	Brain Anterior Caudate	brain
5	chr17:67074600-67083800	Strong transcription	Skeletal Muscle Female	skeletal muscle
6	chr17:67075600-67085600	Strong transcription	Fetal Lung	lung
7	chr17:67076800-67109800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr17:67077600-67082600	Weak transcription	Brain Angular Gyrus	brain
9	chr17:67077800-67137800	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr17:67079000-67082600	Weak transcription	Colonic Mucosa	Colon
11	chr17:67079400-67081800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr17:67079400-67084200	Strong transcription	Adipose Nuclei	Adipose
13	chr17:67079400-67087400	Weak transcription	Colon Smooth Muscle	Colon
14	chr17:67079400-67090600	Weak transcription	Fetal Muscle Trunk	muscle
15	chr17:67079400-67093600	Weak transcription	Fetal Stomach	stomach
16	chr17:67079400-67095600	Weak transcription	Psoas Muscle	Psoas
17	chr17:67079400-67112200	Strong transcription	Liver	Liver
18	chr17:67079400-67112600	Weak transcription	Sigmoid Colon	Sigmoid Colon
19	chr17:67079400-67117600	Weak transcription	Esophagus	oesophagus
20	chr17:67079600-67091600	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr17:67079600-67101200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr17:67079600-67114200	Weak transcription	NHDF-Ad	bronchial
23	chr17:67080000-67085000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr17:67080600-67083600	Weak transcription	Lung	lung
25	chr17:67080600-67086600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr17:67080800-67081800	Weak transcription	Duodenum Smooth Muscle	Duodenum
27	chr17:67080800-67088000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr17:67080800-67088600	Weak transcription	GM12878-XiMat	blood
29	chr17:67080800-67090800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr17:67080800-67112000	Weak transcription	Brain Substantia Nigra	brain
31	chr17:67081200-67086200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr17:67081200-67088200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr17:67081200-67088600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr17:67081200-67090800	Weak transcription	Fetal Muscle Leg	muscle
35	chr17:67081200-67102000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr17:67081400-67089400	Weak transcription	Ovary	ovary
37	chr17:67081400-67090400	Weak transcription	Left Ventricle	heart
38	chr17:67081400-67095000	Weak transcription	Stomach Smooth Muscle	stomach
39	chr17:67081400-67118600	Weak transcription	Right Ventricle	heart
40	chr17:67081800-67082200	Strong transcription	Duodenum Smooth Muscle	Duodenum
41	chr17:67082200-67114400	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr17:67083800-67090200	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr17:67084200-67089000	Weak transcription	Adipose Nuclei	Adipose
44	chr17:67084600-67085000	Enhancers	K562	blood
45	chr17:67085000-67086600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
46	chr17:67085600-67088600	Weak transcription	Fetal Lung	lung
47	chr17:67085800-67099600	Weak transcription	Lung	lung
48	chr17:67086200-67087000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr17:67086400-67087400	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr17:67086600-67087000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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