Variant report

Variant	esv3427395
Chromosome Location	chr9:27025338-27040548
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr9:27033873-27034153	K562	blood:	n/a	n/a
2	ARID3A	chr9:27033859-27034180	HepG2	liver:	n/a	n/a
3	BHLHE40	chr9:27033947-27034178	GM12878	blood:	n/a	n/a
4	CEBPB	chr9:27033872-27034187	Hela-S3	cervix:	n/a	n/a
5	CHD1	chr9:27033812-27034364	IMR90	lung:	n/a	n/a
6	CTCF	chr9:27033940-27034090	GM12878	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
7	CTCF	chr9:27033920-27034070	GM06990	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
8	CTCF	chr9:27033625-27033667	Kidney_OC	kidney:	n/a	n/a
9	CTCF	chr9:27033900-27034050	HL-60	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
10	CTCF	chr9:27033911-27034061	GM19240	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
11	CTCF	chr9:27033940-27034090	HCFaa	heart:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
12	CTCF	chr9:27033887-27034122	GM10266	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
13	CTCF	chr9:27033900-27034050	RPTEC	kidney:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
14	CTCF	chr9:27033920-27034070	GM12875	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
15	CTCF	chr9:27033920-27034070	HVMF	connective:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
16	CTCF	chr9:27033830-27034137	A549	lung:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
17	CTCF	chr9:27033900-27034050	HA-sp	spinal cord:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
18	CTCF	chr9:27033860-27034010	GM12864	blood:	n/a	n/a
19	CTCF	chr9:27033920-27034070	HPAF	blood vessel:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
20	CTCF	chr9:27033862-27034119	Gliobla	brain:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
21	CTCF	chr9:27033900-27034050	AG09309	skin:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
22	CTCF	chr9:27033940-27034090	HFF	foreskin:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
23	CTCF	chr9:27033851-27034146	Spleen_OC	spleen:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
24	CTCF	chr9:27033940-27034090	GM12867	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
25	CTCF	chr9:27033920-27034070	HPF	lung:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
26	CTCF	chr9:27033900-27034050	HFF-Myc	foreskin:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
27	CTCF	chr9:27033900-27034050	GM06990	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
28	CTCF	chr9:27033887-27034097	MCF-7	breast:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
29	CTCF	chr9:27033920-27034070	SAEC	small airway:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
30	CTCF	chr9:27033920-27034070	HMF	breast:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
31	CTCF	chr9:27033858-27034141	Lung_OC	lung:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
32	CTCF	chr9:27033906-27034062	GM19239	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
33	CTCF	chr9:27033600-27033750	HFF-Myc	foreskin:	n/a	n/a
34	CTCF	chr9:27033940-27034090	HCT-116	colon:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
35	CTCF	chr9:27033766-27034139	MCF-7	breast:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
36	CTCF	chr9:27033920-27034070	GM12870	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
37	CTCF	chr9:27033900-27034050	GM12870	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
38	CTCF	chr9:27033892-27034146	GM10248	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
39	CTCF	chr9:27033900-27034050	GM12869	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
40	CTCF	chr9:27033860-27034010	NHEK	skin:	n/a	n/a
41	CTCF	chr9:27033786-27034380	SK-N-SH	brain:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
42	CTCF	chr9:27033940-27034090	HBMEC	blood vessel:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
43	CTCF	chr9:27033940-27034090	HEEpiC	esophagus:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
44	CTCF	chr9:27033840-27033990	GM12864	blood:	n/a	n/a
45	CTCF	chr9:27033900-27034050	BE2_C	brain:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
46	CTCF	chr9:27034020-27034170	HFF-Myc	foreskin:	n/a	n/a
47	CTCF	chr9:27033940-27034090	SK-N-SH_RA	brain:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
48	CTCF	chr9:27033802-27034063	A549	lung:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
49	CTCF	chr9:27033920-27034070	GM12868	blood:	n/a	chr9:27034004-27034017 chr9:27034003-27034024
50	CTCF	chr9:27033900-27034050	Caco-2	colon:	n/a	chr9:27034004-27034017 chr9:27034003-27034024

No.	Distal block	Cell Line	Cell type
1	chr9:27033573..27034169-chr9:27165385..27166023,2	MCF-7	breast:
2	chr9:27033902..27034442-chr9:27247489..27248319,2	MCF-7	breast:
3	chr9:27033540..27034483-chr9:27275947..27276717,3	MCF-7	breast:
4	chr9:27019266..27022191-chr9:27024943..27027796,2	K562	blood:
5	chr9:27033503..27034503-chr9:27276144..27277065,4	K562	blood:
6	chr9:27033695..27036371-chr9:27569729..27572536,2	K562	blood:

Variant related genes	Relation type
IFT74	TF binding region

Extended variants
information (count: 599 )
Associated
traits (count: 124 )

Variant overlapped rSNPs/rCNVs (count:599 , 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	rs11496422	chr9:27025340-27025341	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs549306996	chr9:27025350-27025351	Weak transcription ZNF genes & repeats Strong transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs567224950	chr9:27025371-27025372	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190915755	chr9:27025381-27025382	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138803896	chr9:27025421-27025422	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs10812514	chr9:27025427-27025428	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs57335230	chr9:27025442-27025443	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs79265470	chr9:27025457-27025458	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs183503576	chr9:27025458-27025459	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs55957927	chr9:27025493-27025494	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs145868950	chr9:27025503-27025504	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs549309653	chr9:27025531-27025532	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs561254049	chr9:27025599-27025600	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs572865301	chr9:27025606-27025607	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs540252531	chr9:27025620-27025621	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs564964825	chr9:27025662-27025663	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs148140182	chr9:27025689-27025690	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs551095327	chr9:27025733-27025734	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs563334778	chr9:27025772-27025773	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs530736007	chr9:27025799-27025800	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs113385064	chr9:27025852-27025853	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs567583407	chr9:27025859-27025860	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs200751383	chr9:27025862-27025863	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs534574834	chr9:27025922-27025923	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs374345839	chr9:27025964-27025965	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs571301459	chr9:27025974-27025975	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs7854065	chr9:27026026-27026027	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs538349628	chr9:27026027-27026028	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs557020401	chr9:27026042-27026043	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376688543	chr9:27026093-27026094	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150664407	chr9:27026130-27026131	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs10967670	chr9:27026142-27026143	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs185249632	chr9:27026175-27026176	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs528406658	chr9:27026190-27026191	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558519181	chr9:27026204-27026205	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376790355	chr9:27026286-27026287	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189998783	chr9:27026323-27026324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79131984	chr9:27026373-27026374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563009624	chr9:27026378-27026379	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs4424351	chr9:27026415-27026416	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs542867741	chr9:27026488-27026489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs561096804	chr9:27026508-27026509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs528382497	chr9:27026516-27026517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182971617	chr9:27026570-27026571	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571212142	chr9:27026646-27026647	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111886635	chr9:27026656-27026657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537504363	chr9:27026657-27026658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550367567	chr9:27026658-27026659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7026933	chr9:27026663-27026664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535990075	chr9:27026665-27026666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:124)

Disease	PMID	Source
Breast cancer	16608533	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Hepatocellular carcinoma	16750200	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Cervical cancer	21063398	CNVD
Retinoblastoma	22278416	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Melanoma	18172304	CNVD
Biliary cancer	19435499	CNVD
Gastric cancer	21586687	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myopathy	18421352	CNVD
Neuroblastoma	18664255	CNVD
Acute lymphoblastic leukemia	18957548	CNVD
Myeloproliferative neoplasm	17564968	CNVD
Malignant meningioma	17937814	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	17603634	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oligodendroglial tumors	17285580	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
microdeletion syndrome	16199537	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Cancer	20164919	CNVD
Ovarian cancer	21720365	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21785460	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	21668985	CNVD
Myelodysplastic syndrome	21251322	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	18803288	CNVD
Metanephric adenoma	20802469	CNVD
Developmental delay	21147756	CNVD
Pilocytic astrocytoma	18670637	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Melanoma	22183965	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Non-small cell lung cancer	19010865	CNVD
Myoepithelioma	18604193	CNVD
Acute myeloid leukemia	19651601	CNVD
Coronary Disease	20032323	CNVD
Squamous cell cancer	20885788	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21732550	CNVD
Gastric cancer	22539939	CNVD
Cancer	21183584	CNVD
T-cell lymphomas	19863542	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Metastatic melanoma	18483359	CNVD
Non-small cell lung cancer	20864512	CNVD
Cervical cancer	21062161	CNVD
Acute myeloid leukemia	16864856	CNVD
Glioblastoma	17090523	CNVD
Lung cancer	16773561	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16774939	CNVD
Bladder cancer	19088036	CNVD
Colorectal cancer	16272173	CNVD
Melanoma	16977458	CNVD
Glioblastoma multiforme	17369134	CNVD
Chagasic megaesophagus	20163722	CNVD
Melanoma	19566914	CNVD
Squamous cell cancer	19047905	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Hodgkin''s lymphoma	18179710	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	21251322	CNVD
Oral cancer	21386901	CNVD
Breast cancer	21858162	CNVD
Pancreatic cancer	21811587	CNVD
Barrett''s syndrome	19417022	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
polycythaemia	22829968	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	21364760	CNVD
Glioblastoma multiforme	21525872	CNVD
Epilepsy	22083797	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Autism	20858261	CNVD
Epilepsy	20858261	CNVD
Mental retardation	20858261	CNVD
Cancer	22183965	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:26957200-27026600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
2	chr9:26957200-27040000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr9:26977800-27026000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr9:26985200-27063800	Weak transcription	Primary T helper cells PMA-I stimulated	--
5	chr9:26991800-27058000	Weak transcription	NHDF-Ad	bronchial
6	chr9:27009800-27070000	Weak transcription	Psoas Muscle	Psoas
7	chr9:27011200-27037400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr9:27011600-27026400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr9:27012000-27048800	Weak transcription	HepG2	liver
10	chr9:27012600-27026200	Weak transcription	Placenta	Placenta
11	chr9:27013200-27025400	Weak transcription	HUVEC	blood vessel
12	chr9:27014000-27025800	Weak transcription	Stomach Mucosa	stomach
13	chr9:27014400-27060800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
14	chr9:27014400-27068200	Weak transcription	Fetal Heart	heart
15	chr9:27016000-27025800	Weak transcription	GM12878-XiMat	blood
16	chr9:27016200-27025400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
17	chr9:27017600-27025400	Weak transcription	Placenta Amnion	Placenta Amnion
18	chr9:27018400-27065200	Weak transcription	Osteobl	bone
19	chr9:27018600-27029400	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr9:27018800-27026200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr9:27019200-27061800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr9:27020800-27026200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr9:27022600-27036200	Weak transcription	NHEK	skin
24	chr9:27023400-27025400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
25	chr9:27023400-27025400	Strong transcription	Fetal Lung	lung
26	chr9:27023600-27025400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr9:27023600-27025400	ZNF genes & repeats	Fetal Intestine Small	intestine
28	chr9:27023600-27025400	ZNF genes & repeats	Fetal Stomach	stomach
29	chr9:27023800-27025400	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr9:27023800-27025400	Strong transcription	Primary B cells from cord blood	blood
31	chr9:27023800-27025400	Strong transcription	Brain Substantia Nigra	brain
32	chr9:27023800-27025400	Strong transcription	Fetal Muscle Trunk	muscle
33	chr9:27023800-27025400	Strong transcription	Fetal Muscle Leg	muscle
34	chr9:27023800-27025400	Strong transcription	Fetal Thymus	thymus
35	chr9:27023800-27025600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr9:27023800-27025800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr9:27024000-27025400	Strong transcription	Brain Anterior Caudate	brain
38	chr9:27024000-27025400	Strong transcription	Rectal Mucosa Donor 29	rectum
39	chr9:27024000-27026000	Strong transcription	HSMM	muscle
40	chr9:27024000-27026200	Strong transcription	A549	lung
41	chr9:27024000-27028400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr9:27024200-27025400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr9:27024200-27025400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
44	chr9:27024200-27026200	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr9:27024400-27028600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
46	chr9:27024400-27029400	Weak transcription	Esophagus	oesophagus
47	chr9:27024400-27047200	Weak transcription	Rectal Mucosa Donor 31	rectum
48	chr9:27024400-27053800	Weak transcription	Lung	lung
49	chr9:27024400-27082600	Weak transcription	Gastric	stomach
50	chr9:27024600-27026400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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