Variant report

Variant	esv19725
Chromosome Location	chr17:45115875-45135615
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:293)
CpG islands
(count:123)
Chromatin interactive
region (count:0)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr17:45127603-45127849	GM12878	blood:	n/a	n/a
2	BATF	chr17:45127560-45127755	GM12878	blood:	n/a	n/a
3	BCL11A	chr17:45126159-45126397	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:45125999-45126154	GM12878	blood:	n/a	n/a
5	BCL11A	chr17:45127435-45128324	GM12878	blood:	n/a	n/a
6	BCL11A	chr17:45127623-45127792	GM12878	blood:	n/a	n/a
7	BCL11A	chr17:45127023-45127200	GM12878	blood:	n/a	n/a
8	CTCF	chr17:45129800-45129950	SAEC	small airway:	n/a	n/a
9	EBF1	chr17:45127582-45127804	GM12878	blood:	n/a	n/a
10	EBF1	chr17:45118420-45118630	GM12878	blood:	n/a	n/a
11	EBF1	chr17:45128015-45128266	GM12878	blood:	n/a	n/a
12	EBF1	chr17:45126885-45127082	GM12878	blood:	n/a	chr17:45127021-45127034 chr17:45127023-45127033 chr17:45127023-45127032
13	EBF1	chr17:45127978-45128282	GM12878	blood:	n/a	n/a
14	EP300	chr17:45119165-45119413	GM12878	blood:	n/a	n/a
15	EP300	chr17:45125793-45126372	GM12878	blood:	n/a	n/a
16	EP300	chr17:45129270-45129419	GM12878	blood:	n/a	n/a
17	EP300	chr17:45127569-45127779	GM12878	blood:	n/a	n/a
18	EP300	chr17:45128985-45130054	GM12878	blood:	n/a	n/a
19	EP300	chr17:45126452-45126851	GM12878	blood:	n/a	n/a
20	EP300	chr17:45127075-45128666	GM12878	blood:	n/a	n/a
21	FOSL2	chr17:45129449-45129784	HepG2	liver:	n/a	n/a
22	FOSL2	chr17:45116644-45116986	HepG2	liver:	n/a	n/a
23	FOSL2	chr17:45125846-45128653	HepG2	liver:	n/a	n/a
24	FOSL2	chr17:45135559-45136764	HepG2	liver:	n/a	n/a
25	FOSL2	chr17:45127458-45128193	HepG2	liver:	n/a	n/a
26	FOSL2	chr17:45125983-45126818	HepG2	liver:	n/a	n/a
27	FOSL2	chr17:45128968-45130056	HepG2	liver:	n/a	n/a
28	FOSL2	chr17:45118319-45118621	HepG2	liver:	n/a	n/a
29	FOSL2	chr17:45124277-45124624	HepG2	liver:	n/a	n/a
30	FOSL2	chr17:45130113-45130336	HepG2	liver:	n/a	n/a
31	GABPA	chr17:45126933-45127169	Hela-S3	cervix:	n/a	n/a
32	GABPA	chr17:45127826-45127979	Hela-S3	cervix:	n/a	n/a
33	GABPA	chr17:45125861-45126328	GM12878	blood:	n/a	n/a
34	GABPA	chr17:45124316-45124582	Hela-S3	cervix:	n/a	n/a
35	GABPA	chr17:45127604-45127991	Hela-S3	cervix:	n/a	n/a
36	GABPA	chr17:45125902-45126375	Hela-S3	cervix:	n/a	n/a
37	GABPA	chr17:45129563-45129694	Hela-S3	cervix:	n/a	n/a
38	GATA2	chr17:45126175-45126906	K562	blood:	n/a	chr17:45126646-45126653
39	GATA2	chr17:45127719-45128288	K562	blood:	n/a	n/a
40	GATA2	chr17:45129308-45129878	K562	blood:	n/a	n/a
41	HEY1	chr17:45134041-45134165	HepG2	liver:	n/a	n/a
42	HEY1	chr17:45127935-45128405	HepG2	liver:	n/a	n/a
43	HEY1	chr17:45127615-45127844	K562	blood:	n/a	n/a
44	IRF4	chr17:45127561-45128193	GM12878	blood:	n/a	n/a
45	IRF4	chr17:45126335-45126677	GM12878	blood:	n/a	n/a
46	IRF4	chr17:45117986-45118322	GM12878	blood:	n/a	n/a
47	IRF4	chr17:45127519-45128583	GM12878	blood:	n/a	n/a
48	IRF4	chr17:45128961-45129676	GM12878	blood:	n/a	n/a
49	IRF4	chr17:45125901-45126388	GM12878	blood:	n/a	n/a
50	IRF4	chr17:45129198-45129565	GM12878	blood:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45126661-45126711	GM19239	blood:	n/a
2	chr17:45126661-45126711	GM19239	blood:	n/a
3	chr17:45134721-45134771	AG04450	lung:	fetal
4	chr17:45126661-45126711	MCF10A-Er-Src	breast:	n/a
5	chr17:45134721-45134771	A549	lung:	n/a
6	chr17:45126661-45126711	PFSK-1	brain:	n/a
7	chr17:45126661-45126711	HRCEpiC	kidney:	n/a
8	chr17:45126661-45126711	HCPEpiC	choroid plexus:	n/a
9	chr17:45134721-45134771	H1-hESC	embryonic stem cell:	embryo
10	chr17:45134721-45134771	GM12878	blood:	n/a
11	chr17:45134721-45134771	AG04449	skin:	fetal
12	chr17:45126661-45126711	H1-hESC	embryonic stem cell:	embryo
13	chr17:45134721-45134771	K562	blood:	n/a
14	chr17:45134721-45134771	MCF10A-Er-Src	breast:	n/a
15	chr17:45126661-45126711	SK-N-SH_RA	brain:	n/a
16	chr17:45134721-45134771	BJ	skin:	n/a
17	chr17:45126661-45126711	AG09309	skin:	n/a
18	chr17:45134721-45134771	T-47D	breast:	n/a
19	chr17:45126661-45126711	NB4	blood:	n/a
20	chr17:45134721-45134771	HEEpiC	esophagus:	n/a
21	chr17:45134721-45134771	GM19239	blood:	n/a
22	chr17:45134721-45134771	HCT-116	colon:	n/a
23	chr17:45134721-45134771	RPTEC	kidney:	n/a
24	chr17:45126661-45126711	HAEpiC	amniotic membrane:	n/a
25	chr17:45134721-45134771	HCPEpiC	choroid plexus:	n/a
26	chr17:45134721-45134771	HRPEpiC	eye:	n/a
27	chr17:45134721-45134771	HEK293	kidney:	embryo
28	chr17:45126661-45126711	GM12891	blood:	n/a
29	chr17:45134721-45134771	HAEpiC	amniotic membrane:	n/a
30	chr17:45126661-45126711	BE2_C	brain:	n/a
31	chr17:45134721-45134771	HCM	heart:	n/a
32	chr17:45134721-45134771	AG09309	skin:	n/a
33	chr17:45126661-45126711	IMR90	lung:	fetal
34	chr17:45126661-45126711	SK-N-MC	brain:	n/a
35	chr17:45126661-45126711	SAEC	small airway:	n/a
36	chr17:45126661-45126711	RPTEC	kidney:	n/a
37	chr17:45126661-45126711	NT2-D1	testis:	n/a
38	chr17:45126661-45126711	HUVEC	blood vessel:	n/a
39	chr17:45126661-45126711	PrEC	prostate:	n/a
40	chr17:45126661-45126711	U87	brain:	n/a
41	chr17:45126661-45126711	SKMC	muscle:	n/a
42	chr17:45134721-45134771	GM12891	blood:	n/a
43	chr17:45134721-45134771	PFSK-1	brain:	n/a
44	chr17:45126661-45126711	AoSMC	blood vessel:	n/a
45	chr17:45134721-45134771	HCF	heart:	n/a
46	chr17:45126661-45126711	T-47D	breast:	n/a
47	chr17:45126661-45126711	NHBE	bronchial:	n/a
48	chr17:45126661-45126711	NH-A	brain:	n/a
49	chr17:45134721-45134771	HepG2	liver:	n/a
50	chr17:45134721-45134771	LNCaP	prostate:	n/a

No data

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GOSR2-1	chr17:45119191-45119483	NONHSAT054245
2	lnc-GOSR2-2	chr17:45124167-45124630	NONHSAT054246
3	lnc-RPRML-3	chr17:45129070-45129168	NONHSAT054254
4	lnc-RPRML-3	chr17:45133975-45134119	ENSG00000262879.1
5	lnc-CDC27-3	chr17:45135517-45136457	NONHSAT054275
6	lnc-RPRML-3	chr17:45126241-45127901	NONHSAT054248
7	lnc-GOSR2-2	chr17:45124512-45124630	NONHSAT054231
8	lnc-GOSR2-2	chr17:45131093-45131559	NONHSAT054261
9	lnc-CDC27-2	chr17:45129070-45129168	ENSG00000250104
10	lnc-RPRML-3	chr17:45129892-45131988	NONHSAT054259
11	lnc-GOSR2-2	chr17:45131884-45134124	NONHSAT054246
12	lnc-RPRML-3	chr17:45128652-45128968	NONHSAT054254
13	lnc-GOSR2-2	chr17:45126422-45131777	NONHSAT054246
14	lnc-GOSR2-2	chr17:45131638-45133274	NONHSAT054261
15	lnc-CDC27-2	chr17:45128639-45128968	ENSG00000250104
16	lnc-GOSR2-2	chr17:45126422-45126511	NONHSAT054231

No data

Variant related genes	Relation type
RN7SL270P	TF binding region
RN7SL270P	CpG island
UTP15	miRNA target sites
STARD7	miRNA target sites

Extended variants
information (count: 589 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543681693	chr17:45115938-45115939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563482894	chr17:45115943-45115944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs370280180	chr17:45115966-45115967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs367957532	chr17:45116008-45116009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs576439417	chr17:45116069-45116070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs375384804	chr17:45116070-45116071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs373583407	chr17:45116073-45116074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559372186	chr17:45116173-45116174	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs143487907	chr17:45116352-45116353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200237704	chr17:45116357-45116358	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs568425025	chr17:45116369-45116370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377023664	chr17:45116390-45116391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs184464185	chr17:45116433-45116434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs537076980	chr17:45116527-45116528	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs77385324	chr17:45117246-45117247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs551251862	chr17:45117421-45117422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs571097361	chr17:45117422-45117423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536666137	chr17:45117423-45117424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374303700	chr17:45117451-45117452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs553625554	chr17:45117494-45117495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs572137032	chr17:45117530-45117531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534693786	chr17:45117540-45117541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs554396275	chr17:45117545-45117546	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs574373262	chr17:45117579-45117580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs199723829	chr17:45117627-45117628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs554967513	chr17:45117721-45117722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs75007539	chr17:45117753-45117754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs74750504	chr17:45117780-45117781	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs545563759	chr17:45117868-45117869	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs559135905	chr17:45117886-45117887	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs62073778	chr17:45117912-45117913	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs2684625	chr17:45117913-45117914	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs571647547	chr17:45118753-45118754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs562087459	chr17:45119112-45119113	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200606151	chr17:45119115-45119116	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs537568231	chr17:45119126-45119127	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559005142	chr17:45119158-45119159	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs111649134	chr17:45119366-45119367	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs539233621	chr17:45119401-45119402	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs571098158	chr17:45119436-45119437	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
41	rs533683327	chr17:45119466-45119467	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
42	rs547353835	chr17:45119469-45119470	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
43	rs567050398	chr17:45119520-45119521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536104923	chr17:45119533-45119534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554642210	chr17:45119549-45119550	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs548076450	chr17:45119580-45119581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs568075081	chr17:45119604-45119605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs537007628	chr17:45119644-45119645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556702141	chr17:45119823-45119824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs576689473	chr17:45119949-45119950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

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
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	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
Breast cancer	21858162	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
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21509527	CNVD
Urothelial carcinoma	21177765	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Breast cancer	17142309	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:358 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45075200-45130200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr17:45086000-45129600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr17:45086000-45129600	Weak transcription	Fetal Muscle Leg	muscle
4	chr17:45086800-45129600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr17:45087200-45126600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr17:45087600-45129600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr17:45088600-45128600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr17:45090000-45131600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
9	chr17:45090200-45131000	Weak transcription	Dnd41	blood
10	chr17:45090600-45129600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
11	chr17:45091200-45129600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr17:45094200-45129600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr17:45095000-45130200	Weak transcription	Brain Anterior Caudate	brain
14	chr17:45096200-45131000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr17:45096400-45129600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr17:45096800-45129600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr17:45096800-45129600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr17:45097400-45129600	Weak transcription	Fetal Stomach	stomach
19	chr17:45109600-45129800	Weak transcription	Fetal Thymus	thymus
20	chr17:45119400-45130200	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr17:45120600-45129600	Weak transcription	Fetal Lung	lung
22	chr17:45121400-45142200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr17:45122000-45129600	Weak transcription	Fetal Intestine Small	intestine
24	chr17:45123200-45129600	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr17:45123800-45129600	Weak transcription	Osteobl	bone
26	chr17:45123800-45143600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr17:45124000-45131400	Weak transcription	GM12878-XiMat	blood
28	chr17:45124200-45129600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr17:45124800-45130200	Weak transcription	Primary B cells from peripheral blood	blood
30	chr17:45124800-45130800	Weak transcription	Rectal Mucosa Donor 29	rectum
31	chr17:45125000-45129600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr17:45125000-45129600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr17:45125000-45129600	Weak transcription	Thymus	Thymus
34	chr17:45125000-45130200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr17:45125000-45130200	Weak transcription	Fetal Muscle Trunk	muscle
36	chr17:45125000-45130400	Weak transcription	Rectal Mucosa Donor 31	rectum
37	chr17:45125000-45133400	Weak transcription	Fetal Brain Female	brain
38	chr17:45125200-45129600	Weak transcription	Primary T helper cells fromperipheralblood	blood
39	chr17:45125200-45130800	Weak transcription	Fetal Kidney	kidney
40	chr17:45125200-45132400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr17:45125200-45143600	Weak transcription	HepG2	liver
42	chr17:45125400-45130200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
43	chr17:45125400-45132400	Weak transcription	Right Ventricle	heart
44	chr17:45125400-45133200	Weak transcription	Gastric	stomach
45	chr17:45125400-45133400	Weak transcription	Pancreas	Pancrea
46	chr17:45125400-45143800	Weak transcription	NHLF	lung
47	chr17:45125600-45130200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr17:45125600-45130200	Weak transcription	HMEC	breast
49	chr17:45126200-45129600	Weak transcription	Adipose Nuclei	Adipose
50	chr17:45126600-45127200	Strong transcription	Fetal Adrenal Gland	Adrenal Gland

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