Variant report

Variant	esv1821088
Chromosome Location	chr8:86550638-86831750
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5420)
CpG islands
(count:1160)
Chromatin interactive
region (count:0)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:5420 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:86781659-86782018	K562	blood:	n/a	n/a
2	ATF1	chr8:86572171-86572827	K562	blood:	n/a	n/a
3	ATF1	chr8:86753942-86754130	K562	blood:	n/a	n/a
4	ATF1	chr8:86563552-86563741	K562	blood:	n/a	n/a
5	BATF	chr8:86828620-86829986	GM12878	blood:	n/a	n/a
6	BATF	chr8:86750849-86751205	GM12878	blood:	n/a	n/a
7	BATF	chr8:86808469-86809480	GM12878	blood:	n/a	n/a
8	BATF	chr8:86807334-86807510	GM12878	blood:	n/a	n/a
9	BATF	chr8:86564638-86565178	GM12878	blood:	n/a	n/a
10	BATF	chr8:86801465-86801759	GM12878	blood:	n/a	n/a
11	BATF	chr8:86572676-86573086	GM12878	blood:	n/a	n/a
12	BATF	chr8:86828647-86829959	GM12878	blood:	n/a	n/a
13	BATF	chr8:86786036-86786450	GM12878	blood:	n/a	n/a
14	BATF	chr8:86776795-86778107	GM12878	blood:	n/a	n/a
15	BATF	chr8:86733380-86734367	GM12878	blood:	n/a	n/a
16	BATF	chr8:86557171-86557645	GM12878	blood:	n/a	n/a
17	BATF	chr8:86797322-86799171	GM12878	blood:	n/a	n/a
18	BATF	chr8:86556634-86557157	GM12878	blood:	n/a	n/a
19	BATF	chr8:86571412-86571576	GM12878	blood:	n/a	n/a
20	BATF	chr8:86773996-86774375	GM12878	blood:	n/a	n/a
21	BATF	chr8:86561630-86563893	GM12878	blood:	n/a	n/a
22	BATF	chr8:86808467-86812389	GM12878	blood:	n/a	n/a
23	BATF	chr8:86800330-86800870	GM12878	blood:	n/a	n/a
24	BATF	chr8:86772830-86773722	GM12878	blood:	n/a	n/a
25	BATF	chr8:86773996-86774290	GM12878	blood:	n/a	n/a
26	BATF	chr8:86768804-86772687	GM12878	blood:	n/a	n/a
27	BATF	chr8:86730444-86733371	GM12878	blood:	n/a	n/a
28	BATF	chr8:86750330-86750624	GM12878	blood:	n/a	n/a
29	BATF	chr8:86751933-86755034	GM12878	blood:	n/a	n/a
30	BATF	chr8:86799176-86799585	GM12878	blood:	n/a	n/a
31	BATF	chr8:86788961-86790252	GM12878	blood:	n/a	n/a
32	BATF	chr8:86560585-86564464	GM12878	blood:	n/a	n/a
33	BATF	chr8:86819527-86819703	GM12878	blood:	n/a	n/a
34	BATF	chr8:86758099-86758263	GM12878	blood:	n/a	n/a
35	BATF	chr8:86758427-86759775	GM12878	blood:	n/a	n/a
36	BATF	chr8:86831488-86831652	GM12878	blood:	n/a	n/a
37	BATF	chr8:86565619-86566067	GM12878	blood:	n/a	n/a
38	BATF	chr8:86824701-86825578	GM12878	blood:	n/a	n/a
39	BATF	chr8:86729434-86730326	GM12878	blood:	n/a	n/a
40	BATF	chr8:86796277-86800156	GM12878	blood:	n/a	n/a
41	BATF	chr8:86816505-86817768	GM12878	blood:	n/a	n/a
42	BATF	chr8:86803935-86804099	GM12878	blood:	n/a	n/a
43	BATF	chr8:86768806-86769818	GM12878	blood:	n/a	n/a
44	BATF	chr8:86812492-86813384	GM12878	blood:	n/a	n/a
45	BATF	chr8:86559441-86559628	GM12878	blood:	n/a	n/a
46	BATF	chr8:86780999-86784881	GM12878	blood:	n/a	n/a
47	BATF	chr8:86557168-86557577	GM12878	blood:	n/a	n/a
48	BATF	chr8:86801465-86801844	GM12878	blood:	n/a	n/a
49	BATF	chr8:86575381-86576452	GM12878	blood:	n/a	n/a
50	BATF	chr8:86568243-86568407	GM12878	blood:	n/a	n/a

(count:1160 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:86556749-86556799	A549	lung:	n/a
2	chr8:86556749-86556799	A549	lung:	n/a
3	chr8:86567383-86567433	HEEpiC	esophagus:	n/a
4	chr8:86564548-86564598	HL-60	blood:	n/a
5	chr8:86568163-86568213	AG04449	skin:	fetal
6	chr8:86556176-86556226	T-47D	breast:	n/a
7	chr8:86568090-86568140	SK-N-SH_RA	brain:	n/a
8	chr8:86568090-86568140	PANC-1	pancreas:	n/a
9	chr8:86551492-86551542	HRE	kidney:	n/a
10	chr8:86551492-86551542	HRPEpiC	eye:	n/a
11	chr8:86574449-86574499	RPTEC	kidney:	n/a
12	chr8:86564548-86564598	BE2_C	brain:	n/a
13	chr8:86574469-86574519	RPTEC	kidney:	n/a
14	chr8:86560192-86560242	IMR90	lung:	fetal
15	chr8:86574469-86574519	HRCEpiC	kidney:	n/a
16	chr8:86556903-86556953	HEK293	kidney:	embryo
17	chr8:86556903-86556953	AG04449	skin:	fetal
18	chr8:86556164-86556214	HRCEpiC	kidney:	n/a
19	chr8:86556749-86556799	BJ	skin:	n/a
20	chr8:86574449-86574499	K562	blood:	n/a
21	chr8:86574449-86574499	HCT-116	colon:	n/a
22	chr8:86572367-86572417	T-47D	breast:	n/a
23	chr8:86572367-86572417	U87	brain:	n/a
24	chr8:86568090-86568140	IMR90	lung:	fetal
25	chr8:86556164-86556214	SK-N-SH_RA	brain:	n/a
26	chr8:86567383-86567433	PFSK-1	brain:	n/a
27	chr8:86556164-86556214	HEK293	kidney:	embryo
28	chr8:86568078-86568128	BJ	skin:	n/a
29	chr8:86786605-86786655	AG10803	skin:	n/a
30	chr8:86564548-86564598	BJ	skin:	n/a
31	chr8:86556164-86556214	NHBE	bronchial:	n/a
32	chr8:86573821-86573871	Hela-S3	cervix:	n/a
33	chr8:86556176-86556226	GM12892	blood:	n/a
34	chr8:86560192-86560242	Hepatocyte	liver:	n/a
35	chr8:86556164-86556214	Jurkat	blood:	n/a
36	chr8:86568078-86568128	Jurkat	blood:	n/a
37	chr8:86560192-86560242	HPAEpiC	pulmonary alveolar:	n/a
38	chr8:86567383-86567433	SK-N-SH_RA	brain:	n/a
39	chr8:86568078-86568128	A549	lung:	n/a
40	chr8:86564548-86564598	NHBE	bronchial:	n/a
41	chr8:86554888-86554938	SK-N-SH_RA	brain:	n/a
42	chr8:86574449-86574499	HEK293	kidney:	embryo
43	chr8:86556164-86556214	MCF10A-Er-Src	breast:	n/a
44	chr8:86568078-86568128	NH-A	brain:	n/a
45	chr8:86574469-86574519	Jurkat	blood:	n/a
46	chr8:86568078-86568128	AG10803	skin:	n/a
47	chr8:86572367-86572417	MCF10A-Er-Src	breast:	n/a
48	chr8:86560192-86560242	K562	blood:	n/a
49	chr8:86568163-86568213	PrEC	prostate:	n/a
50	chr8:86564548-86564598	HCM	heart:	n/a

No data

Variant related genes	Relation type
REXO1L11P	TF binding region
REXO1L1P	TF binding region
REXO1L10P	TF binding region
REXO1L12P	TF binding region
REXO1L9P	TF binding region
REXO1L3P	TF binding region
REXO1L8P	TF binding region
REXO1L11P	CpG island
REXO1L1P	CpG island
REXO1L10P	CpG island
REXO1L12P	CpG island
REXO1L9P	CpG island
REXO1L3P	CpG island
REXO1L8P	CpG island

Extended variants
information (count: 914 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:914 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185410051	chr8:86550673-86550674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs544233623	chr8:86550681-86550682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs561275166	chr8:86550719-86550720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187530197	chr8:86550737-86550738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs115903635	chr8:86550782-86550783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs192055108	chr8:86550806-86550807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532313029	chr8:86550809-86550810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs552371068	chr8:86550817-86550818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147884040	chr8:86550866-86550867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531447030	chr8:86550873-86550874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs545579075	chr8:86550881-86550882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs567714273	chr8:86550920-86550921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533569586	chr8:86550952-86550953	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs377654412	chr8:86550953-86550954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs56011231	chr8:86550966-86550967	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs184246150	chr8:86551014-86551015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs572113413	chr8:86551037-86551038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538828097	chr8:86551075-86551076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs376195395	chr8:86551079-86551080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs115264198	chr8:86551103-86551104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs538325916	chr8:86551122-86551123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188799681	chr8:86551123-86551124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs141421950	chr8:86551140-86551141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540647041	chr8:86551164-86551165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542289649	chr8:86551173-86551174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs181191974	chr8:86551183-86551184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184660379	chr8:86551192-86551193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377698439	chr8:86551201-86551202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531454496	chr8:86551237-86551238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547856984	chr8:86551253-86551254	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs189130767	chr8:86551268-86551269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs527256836	chr8:86551287-86551288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547008985	chr8:86551309-86551310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566776615	chr8:86551329-86551330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs560569861	chr8:86551341-86551342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs531193846	chr8:86551367-86551368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539328551	chr8:86551372-86551373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs182425797	chr8:86551379-86551380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs569430605	chr8:86551402-86551403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538090760	chr8:86551418-86551419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555067283	chr8:86551457-86551458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs575008054	chr8:86551492-86551493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534137272	chr8:86551496-86551497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs577002280	chr8:86551498-86551499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554220020	chr8:86551502-86551503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371043493	chr8:86551512-86551513	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs138112003	chr8:86551543-86551544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546077525	chr8:86551558-86551559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs556210971	chr8:86551599-86551600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543342225	chr8:86551643-86551644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
small cell lung cancer	20016488	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
Epilepsy	20502679	CNVD
Acute monocytic leukemia	16498392	CNVD
Autism	20841430	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:86548800-86552800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:86552800-86553000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:86563400-86563800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr8:86563600-86563800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:86563800-86572200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr8:86564200-86564400	Weak transcription	Spleen	Spleen
7	chr8:86566200-86567800	Weak transcription	Pancreas	Pancrea
8	chr8:86567400-86567800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr8:86567400-86567800	Weak transcription	Spleen	Spleen
10	chr8:86567400-86568000	Weak transcription	Left Ventricle	heart
11	chr8:86567800-86568000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr8:86567800-86568200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr8:86567800-86568200	ZNF genes & repeats	Gastric	stomach
14	chr8:86567800-86568200	ZNF genes & repeats	Pancreas	Pancrea
15	chr8:86567800-86568200	ZNF genes & repeats	Spleen	Spleen
16	chr8:86568000-86568200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
17	chr8:86568000-86568200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr8:86568000-86568200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr8:86568000-86568200	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
20	chr8:86568000-86568200	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
21	chr8:86568000-86568200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
22	chr8:86568000-86568200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr8:86568000-86568200	ZNF genes & repeats	Esophagus	oesophagus
24	chr8:86568000-86568200	ZNF genes & repeats	Ovary	ovary
25	chr8:86568000-86568200	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
26	chr8:86568000-86568200	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
27	chr8:86568000-86568200	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
28	chr8:86568200-86569600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr8:86568200-86569600	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr8:86568200-86572000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr8:86568200-86572200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr8:86568200-86572200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr8:86568200-86572200	Weak transcription	Skeletal Muscle Male	skeletal muscle
34	chr8:86568400-86569800	Weak transcription	Ovary	ovary
35	chr8:86569600-86570000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:86569600-86570000	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
37	chr8:86569800-86570000	Weak transcription	Left Ventricle	heart
38	chr8:86570000-86570600	Weak transcription	Ovary	ovary
39	chr8:86570000-86572000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr8:86570000-86572200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr8:86570200-86571600	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr8:86570200-86572000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
43	chr8:86571800-86572000	Weak transcription	Left Ventricle	heart
44	chr8:86571800-86572200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr8:86572000-86572800	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
46	chr8:86572000-86572800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
47	chr8:86572000-86572800	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
48	chr8:86572000-86572800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
49	chr8:86572200-86572400	ZNF genes & repeats	Left Ventricle	heart
50	chr8:86572200-86572600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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