Variant report

Variant	esv10233
Chromosome Location	chr17:15632283-15677380
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:146)
CpG islands
(count:1039)
Chromatin interactive
region (count:2)
LncRNA
region (count:30)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:146 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr17:15634010-15634038	K562	blood:	n/a	n/a
2	CEBPB	chr17:15643389-15643669	A549	lung:	n/a	n/a
3	CEBPB	chr17:15643479-15643633	Hela-S3	cervix:	n/a	n/a
4	CTCF	chr17:15672366-15672430	K562	blood:	n/a	n/a
5	CTCF	chr17:15677202-15677291	GM20000	blood:	n/a	n/a
6	CTCF	chr17:15645940-15646090	NHEK	skin:	n/a	n/a
7	CTCF	chr17:15643440-15643590	HVMF	connective:	n/a	n/a
8	CTCF	chr17:15672266-15672501	MCF-7	breast:	n/a	n/a
9	CTCF	chr17:15672282-15672499	GM12892	blood:	n/a	n/a
10	CTCF	chr17:15672262-15672511	MCF-7	breast:	n/a	n/a
11	CTCF	chr17:15643480-15643630	HPAF	blood vessel:	n/a	n/a
12	CTCF	chr17:15672228-15672496	A549	lung:	n/a	n/a
13	CTCF	chr17:15643500-15643650	MCF-7	breast:	n/a	n/a
14	CTCF	chr17:15643510-15643594	Hela-S3	cervix:	n/a	n/a
15	CTCF	chr17:15643500-15643650	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr17:15672291-15672439	LNCaP	prostate:	n/a	n/a
17	CTCF	chr17:15642690-15642735	GM20000	blood:	n/a	n/a
18	CTCF	chr17:15672277-15672498	Gliobla	brain:	n/a	n/a
19	CTCF	chr17:15643500-15643650	HEK293	kidney:	n/a	n/a
20	CTCF	chr17:15672365-15672431	GM19239	blood:	n/a	n/a
21	CTCF	chr17:15672264-15672508	MCF-7	breast:	n/a	n/a
22	CTCF	chr17:15671235-15671316	GM13977	blood:	n/a	n/a
23	CTCF	chr17:15672313-15672454	GM19240	blood:	n/a	n/a
24	CTCF	chr17:15672330-15672420	GM19238	blood:	n/a	n/a
25	CTCF	chr17:15643480-15643630	NHEK	skin:	n/a	n/a
26	CTCF	chr17:15643133-15643184	Kidney_OC	kidney:	n/a	n/a
27	CTCF	chr17:15677252-15677352	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr17:15672440-15672590	HFF-Myc	foreskin:	n/a	n/a
29	CTCF	chr17:15643460-15643610	HMF	breast:	n/a	n/a
30	CTCF	chr17:15643520-15643670	HCFaa	heart:	n/a	n/a
31	CTCF	chr17:15666698-15666753	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr17:15672295-15672488	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr17:15641806-15641845	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr17:15672364-15672419	Medullo	brain:	n/a	n/a
35	CTCF	chr17:15654856-15654909	GM13976	blood:	n/a	n/a
36	CTCF	chr17:15672311-15672497	Fibrobl	skin:	n/a	n/a
37	CTCF	chr17:15653788-15653894	LNCaP	prostate:	n/a	n/a
38	CTCF	chr17:15643498-15643612	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr17:15672250-15672516	GM12878	blood:	n/a	n/a
40	CTCF	chr17:15643460-15643610	HMEC	breast:	n/a	n/a
41	CTCF	chr17:15672060-15672210	HAc	cerebellar:	n/a	n/a
42	CTCF	chr17:15643520-15643670	HEK293	kidney:	n/a	n/a
43	CTCF	chr17:15643500-15643650	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr17:15653545-15653592	GM13976	blood:	n/a	n/a
45	CTCF	chr17:15672328-15672471	HepG2	liver:	n/a	n/a
46	CTCF	chr17:15655205-15655263	GM13977	blood:	n/a	n/a
47	CTCF	chr17:15672304-15672497	Pancreas_OC	pancreas:	n/a	n/a
48	CTCF	chr17:15672290-15672483	A549	lung:	n/a	n/a
49	CTCF	chr17:15640241-15640287	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr17:15636557-15636611	Kidney_OC	kidney:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15655637-15655687	AG10803	skin:	n/a
2	chr17:15635431-15635481	GM12892	blood:	n/a
3	chr17:15655637-15655687	AG10803	skin:	n/a
4	chr17:15635431-15635481	GM12892	blood:	n/a
5	chr17:15634511-15634561	AG09309	skin:	n/a
6	chr17:15635376-15635426	H1-hESC	embryonic stem cell:	embryo
7	chr17:15644575-15644625	NH-A	brain:	n/a
8	chr17:15653473-15653523	HepG2	liver:	n/a
9	chr17:15653473-15653523	HUVEC	blood vessel:	n/a
10	chr17:15646415-15646465	ovcar-3	ovarian:	n/a
11	chr17:15653473-15653523	AG09309	skin:	n/a
12	chr17:15635401-15635451	AG04449	skin:	fetal
13	chr17:15655637-15655687	RPTEC	kidney:	n/a
14	chr17:15635468-15635518	HCPEpiC	choroid plexus:	n/a
15	chr17:15652715-15652765	NB4	blood:	n/a
16	chr17:15635431-15635481	Hepatocyte	liver:	n/a
17	chr17:15652715-15652765	AG10803	skin:	n/a
18	chr17:15650385-15650435	AG04450	lung:	fetal
19	chr17:15634721-15634771	SK-N-SH_RA	brain:	n/a
20	chr17:15644575-15644625	MCF-7	breast:	n/a
21	chr17:15646415-15646465	AG10803	skin:	n/a
22	chr17:15650385-15650435	HNPCEpiC	eye:	n/a
23	chr17:15652329-15652379	HCPEpiC	choroid plexus:	n/a
24	chr17:15635376-15635426	PrEC	prostate:	n/a
25	chr17:15635401-15635451	IMR90	lung:	fetal
26	chr17:15635464-15635514	HCT-116	colon:	n/a
27	chr17:15634721-15634771	HEEpiC	esophagus:	n/a
28	chr17:15653473-15653523	MCF-7	breast:	n/a
29	chr17:15652854-15652904	U87	brain:	n/a
30	chr17:15652854-15652904	MCF10A-Er-Src	breast:	n/a
31	chr17:15634511-15634561	PrEC	prostate:	n/a
32	chr17:15652854-15652904	ovcar-3	ovarian:	n/a
33	chr17:15653096-15653146	HRPEpiC	eye:	n/a
34	chr17:15646415-15646465	SK-N-SH	brain:	n/a
35	chr17:15635468-15635518	ovcar-3	ovarian:	n/a
36	chr17:15653096-15653146	AG04449	skin:	fetal
37	chr17:15653473-15653523	H1-hESC	embryonic stem cell:	embryo
38	chr17:15652329-15652379	BE2_C	brain:	n/a
39	chr17:15634511-15634561	ovcar-3	ovarian:	n/a
40	chr17:15653548-15653598	SAEC	small airway:	n/a
41	chr17:15635376-15635426	SKMC	muscle:	n/a
42	chr17:15635376-15635426	HRPEpiC	eye:	n/a
43	chr17:15635401-15635451	HUVEC	blood vessel:	n/a
44	chr17:15653096-15653146	ovcar-3	ovarian:	n/a
45	chr17:15635431-15635481	IMR90	lung:	fetal
46	chr17:15635468-15635518	AG09309	skin:	n/a
47	chr17:15653096-15653146	HRCEpiC	kidney:	n/a
48	chr17:15652854-15652904	HEEpiC	esophagus:	n/a
49	chr17:15635401-15635451	LNCaP	prostate:	n/a
50	chr17:15644575-15644625	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15646677..15648283-chr17:15650856..15653224,2	K562	blood:
2	chr17:15646677..15648283-chr17:15650856..15653224,2	K562	blood:

(count:30 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIM16-1	chr17:15643410-15648034	NONHSAT145863
2	lnc-TRIM16-6	chr17:15661567-15661668	NONHSAT145865
3	lnc-TRIM16-7	chr17:15663778-15664123	NONHSAT145868
4	lnc-TRIM16-3	chr17:15666900-15667083	ENSG00000233193
5	lnc-ZNF286A-7	chr17:15637159-15637402	NONHSAT145859
6	lnc-TRIM16-6	chr17:15650705-15650937	NONHSAT145865
7	lnc-TRIM16-1	chr17:15649993-15650081	NONHSAT145863
8	lnc-ZNF286A-7	chr17:15637028-15637251	NONHSAT145856
9	lnc-ZNF286A-7	chr17:15638018-15638351	NONHSAT145859
10	lnc-ZNF286A-7	chr17:15637356-15637402	NONHSAT145856
11	lnc-TRIM16-6	chr17:15661567-15661699	ucscGeneNc_uc010cow_1
12	lnc-TRIM16-3	chr17:15664928-15665158	ENSG00000233193
13	lnc-ZNF286A-7	chr17:15638047-15638347	NONHSAT145858
14	lnc-TRIM16-7	chr17:15664746-15664857	NONHSAT145868
15	lnc-ZNF286A-7	chr17:15638018-15638177	NONHSAT145856
16	lnc-TRIM16-6	chr17:15660004-15660081	ucscGeneNc_uc010cow_1
17	lnc-TRIM16-6	chr17:15650514-15650937	ucscGeneNc_uc010cow_1
18	lnc-ZNF286A-7	chr17:15635622-15635698	NONHSAT145858
19	lnc-TRIM16-1	chr17:15638337-15638689	ENSG00000233002.2
20	lnc-TRIM16-1	chr17:15641817-15642103	ENSG00000233002.2
21	lnc-TRIM16-2	chr17:15643942-15644050	ENSG00000233002.2
22	lnc-TRIM16-1	chr17:15666900-15669134	NONHSAT145863
23	lnc-TRIM16-2	chr17:15652075-15652506	ENSG00000233002.2
24	lnc-TRIM16-1	chr17:15639034-15639149	ENSG00000233002.2
25	lnc-TRIM16-1	chr17:15652017-15652629	NONHSAT145866
26	lnc-TRIM16-1	chr17:15646917-15647105	ENSG00000233002.2
27	lnc-ZNF286A-7	chr17:15635571-15635698	NONHSAT145856
28	lnc-TRIM16-1	chr17:15646917-15647113	ENSG00000233002.2
29	lnc-TRIM16-1	chr17:15639776-15639863	ENSG00000233002.2
30	lnc-TRIM16-6	chr17:15660004-15660081	NONHSAT145865

No data

Variant related genes	Relation type
ENSG00000233002	TF binding region
ZSWIM5P1	TF binding region
CDRT15P2	TF binding region
ENSG00000233193	TF binding region
ENSG00000267227	TF binding region
TBC1D26	TF binding region
ENSG00000233002	CpG island
ZSWIM5P1	CpG island
CDRT15P2	CpG island
ENSG00000233193	CpG island
ENSG00000267227	CpG island
TBC1D26	CpG island
ENSG00000233002	chromatin interactions
ENSG00000267227	chromatin interactions

Extended variants
information (count: 1248 )
Associated
traits (count: 128 )

Variant overlapped rSNPs/rCNVs (count:1248 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs62072371	chr17:15632335-15632336	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
2	rs190256151	chr17:15632337-15632338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180818755	chr17:15632355-15632356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs71228182	chr17:15632371-15632372	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs558392023	chr17:15632377-15632378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs71228654	chr17:15632383-15632384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574429240	chr17:15632396-15632397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs71228183	chr17:15632419-15632420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62072372	chr17:15632450-15632451	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs554498205	chr17:15632477-15632478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs574864486	chr17:15632478-15632479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs532716427	chr17:15632481-15632482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142691127	chr17:15632488-15632489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185177592	chr17:15632499-15632500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528499154	chr17:15632509-15632510	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs71228655	chr17:15632530-15632531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190823142	chr17:15632582-15632583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs55712722	chr17:15632584-15632585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs568566323	chr17:15632602-15632603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs71228184	chr17:15632614-15632615	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12600753	chr17:15632653-15632654	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs569862495	chr17:15632655-15632656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538791549	chr17:15632658-15632659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370454966	chr17:15632715-15632716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554307947	chr17:15632739-15632740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577267207	chr17:15632744-15632745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538850965	chr17:15632761-15632762	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554253199	chr17:15632788-15632789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs141755794	chr17:15632800-15632801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs199694538	chr17:15632806-15632807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556595375	chr17:15632854-15632855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577029361	chr17:15632867-15632868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184108144	chr17:15632868-15632869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs150551966	chr17:15632870-15632871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7209624	chr17:15632878-15632879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs28711815	chr17:15632894-15632895	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
37	rs28582226	chr17:15632895-15632896	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs7208315	chr17:15632920-15632921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531073088	chr17:15632975-15632976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs551097284	chr17:15632989-15632990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570924324	chr17:15632995-15632996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532369921	chr17:15632999-15633000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552065095	chr17:15633022-15633023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371484365	chr17:15633048-15633049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534605528	chr17:15633064-15633065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548216839	chr17:15633071-15633072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs567723653	chr17:15633081-15633082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs536611462	chr17:15633082-15633083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs377263788	chr17:15633088-15633089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs146327760	chr17:15633109-15633110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:128)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15627200-15636600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr17:15634000-15639200	Weak transcription	Fetal Stomach	stomach
3	chr17:15634800-15636600	Enhancers	Placenta	Placenta
4	chr17:15635000-15635200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr17:15636600-15637000	Weak transcription	Placenta	Placenta
6	chr17:15636600-15637400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr17:15637000-15638800	Enhancers	Placenta	Placenta
8	chr17:15637400-15647400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr17:15638800-15639200	Weak transcription	Placenta	Placenta
10	chr17:15639200-15639400	Enhancers	Placenta	Placenta
11	chr17:15639400-15646400	Weak transcription	Placenta	Placenta
12	chr17:15641800-15642000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr17:15642000-15644200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr17:15644000-15644200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr17:15644200-15646000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr17:15645200-15646400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
17	chr17:15645600-15646000	Flanking Active TSS	Lung	lung
18	chr17:15646000-15647600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr17:15646000-15647600	Weak transcription	Lung	lung
20	chr17:15646400-15648400	Enhancers	Placenta	Placenta
21	chr17:15647400-15648800	Enhancers	Ovary	ovary
22	chr17:15647400-15649000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr17:15647400-15649000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr17:15647600-15647800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr17:15647600-15648000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr17:15647600-15648000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr17:15647600-15648400	Enhancers	Fetal Muscle Leg	muscle
28	chr17:15647600-15648400	Enhancers	Lung	lung
29	chr17:15647800-15649000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
30	chr17:15648000-15648400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr17:15648000-15648600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr17:15648000-15648800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr17:15648200-15648800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr17:15648200-15648800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
35	chr17:15648200-15649000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr17:15648800-15652800	Weak transcription	Ovary	ovary
37	chr17:15651400-15651800	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr17:15651400-15651800	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr17:15652600-15653000	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
40	chr17:15652800-15653000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr17:15652800-15653000	Flanking Active TSS	Ovary	ovary
42	chr17:15652800-15653000	Flanking Active TSS	Psoas Muscle	Psoas
43	chr17:15652800-15653200	Enhancers	Placenta Amnion	Placenta Amnion
44	chr17:15652800-15653400	Active TSS	Right Ventricle	heart
45	chr17:15653000-15654000	Active TSS	Ovary	ovary
46	chr17:15671800-15672000	Enhancers	Fetal Muscle Leg	muscle
47	chr17:15672000-15672800	Weak transcription	Fetal Muscle Leg	muscle
48	chr17:15672000-15673200	Enhancers	Fetal Muscle Trunk	muscle
49	chr17:15672600-15674200	Enhancers	Stomach Smooth Muscle	stomach
50	chr17:15672800-15673000	Bivalent Enhancer	Fetal Stomach	stomach

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