Variant report

Variant	esv3499772
Chromosome Location	chr6:165715090-165732713
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:51)
CpG islands
(count:611)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:51 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr6:165722731-165723055	Hela-S3	cervix:	n/a	n/a
2	CHD2	chr6:165722861-165723245	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr6:165722820-165722970	HCPEpiC	choroid plexus:	n/a	n/a
4	E2F6	chr6:165722059-165723307	H1-hESC	embryonic stem cell:	n/a	chr6:165722645-165722660
5	E2F6	chr6:165722358-165722715	A549	lung:	n/a	chr6:165722645-165722660
6	E2F6	chr6:165722373-165722547	K562	blood:	n/a	n/a
7	E2F6	chr6:165722203-165723274	H1-hESC	embryonic stem cell:	n/a	chr6:165722645-165722660
8	ELK1	chr6:165722938-165722976	Hela-S3	cervix:	n/a	n/a
9	GATA2	chr6:165721218-165721628	SH-SY5Y	brain:	n/a	n/a
10	HA-E2F1	chr6:165722465-165723210	MCF-7	breast:	n/a	chr6:165722645-165722660
11	JUN	chr6:165723053-165723253	H1-hESC	embryonic stem cell:	n/a	n/a
12	JUND	chr6:165722959-165723157	H1-hESC	embryonic stem cell:	n/a	n/a
13	JUND	chr6:165722982-165723148	H1-hESC	embryonic stem cell:	n/a	n/a
14	KAP1	chr6:165722299-165723318	HEK293	kidney:	n/a	n/a
15	KAP1	chr6:165722694-165723255	U2OS	brain:	n/a	n/a
16	MAX	chr6:165722435-165722541	A549	lung:	n/a	n/a
17	MAX	chr6:165722597-165723090	A549	lung:	n/a	n/a
18	MAX	chr6:165722256-165723257	H1-hESC	embryonic stem cell:	n/a	n/a
19	MAX	chr6:165722210-165723123	A549	lung:	n/a	n/a
20	MAX	chr6:165722452-165723119	Hela-S3	cervix:	n/a	n/a
21	MAX	chr6:165722235-165723305	H1-hESC	embryonic stem cell:	n/a	n/a
22	MAX	chr6:165722322-165723199	H1-hESC	embryonic stem cell:	n/a	n/a
23	MAZ	chr6:165722769-165722825	Hela-S3	cervix:	n/a	n/a
24	MAZ	chr6:165722656-165723287	IMR90	lung:	n/a	n/a
25	MAZ	chr6:165720108-165720147	HepG2	liver:	n/a	n/a
26	MXI1	chr6:165722399-165723472	SK-N-SH	brain:	n/a	chr6:165723107-165723122 chr6:165723109-165723124
27	MXI1	chr6:165723072-165723238	Hela-S3	cervix:	n/a	chr6:165723107-165723122 chr6:165723109-165723124
28	MXI1	chr6:165722600-165722785	Hela-S3	cervix:	n/a	n/a
29	MXI1	chr6:165722535-165723262	IMR90	lung:	n/a	chr6:165723107-165723122 chr6:165723109-165723124
30	MXI1	chr6:165722586-165723269	H1-hESC	embryonic stem cell:	n/a	chr6:165723107-165723122 chr6:165723109-165723124
31	MYC	chr6:165722714-165722893	MCF-7	breast:	n/a	n/a
32	MYC	chr6:165722509-165722539	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr6:165720149-165720201	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr6:165722619-165723296	H1-neurons	neurons:	n/a	n/a
35	POLR2A	chr6:165722942-165723162	H1-hESC	embryonic stem cell:	n/a	n/a
36	POLR2A	chr6:165722616-165723253	H1-neurons	neurons:	n/a	n/a
37	REST	chr6:165730334-165730521	H1-hESC	embryonic stem cell:	n/a	chr6:165730431-165730441 chr6:165730435-165730444
38	REST	chr6:165730351-165730533	H1-hESC	embryonic stem cell:	n/a	chr6:165730431-165730441 chr6:165730435-165730444
39	SIN3A	chr6:165722471-165723351	H1-hESC	embryonic stem cell:	n/a	chr6:165723168-165723181
40	SIN3AK20	chr6:165722871-165723214	PFSK-1	brain:	n/a	n/a
41	SIN3AK20	chr6:165722964-165723285	H1-hESC	embryonic stem cell:	n/a	n/a
42	SIN3AK20	chr6:165722835-165723333	H1-hESC	embryonic stem cell:	n/a	n/a
43	SIN3AK20	chr6:165722748-165723232	PFSK-1	brain:	n/a	n/a
44	SP1	chr6:165722791-165723291	H1-hESC	embryonic stem cell:	n/a	chr6:165722817-165722827
45	STAT3	chr6:165723521-165723608	MCF10A-Er-Src	breast:	n/a	n/a
46	TEAD4	chr6:165722860-165723219	H1-hESC	embryonic stem cell:	n/a	n/a
47	TEAD4	chr6:165722906-165723294	H1-hESC	embryonic stem cell:	n/a	n/a
48	YY1	chr6:165722887-165723220	H1-hESC	embryonic stem cell:	n/a	n/a
49	YY1	chr6:165722731-165723222	H1-hESC	embryonic stem cell:	n/a	n/a
50	ZNF143	chr6:165722814-165723314	H1-hESC	embryonic stem cell:	n/a	chr6:165723215-165723234

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165715592-165715642	PrEC	prostate:	n/a
2	chr6:165715592-165715642	PrEC	prostate:	n/a
3	chr6:165715586-165715636	BE2_C	brain:	n/a
4	chr6:165715592-165715642	H1-hESC	embryonic stem cell:	embryo
5	chr6:165715586-165715636	HCPEpiC	choroid plexus:	n/a
6	chr6:165715240-165715290	HCF	heart:	n/a
7	chr6:165723708-165723758	HL-60	blood:	n/a
8	chr6:165715757-165715807	SAEC	small airway:	n/a
9	chr6:165715586-165715636	GM19239	blood:	n/a
10	chr6:165722651-165722701	ECC-1	luminal epithelium:	n/a
11	chr6:165715586-165715636	HCF	heart:	n/a
12	chr6:165715586-165715636	MCF-7	breast:	n/a
13	chr6:165723708-165723758	Jurkat	blood:	n/a
14	chr6:165723034-165723084	SK-N-SH_RA	brain:	n/a
15	chr6:165715240-165715290	HEEpiC	esophagus:	n/a
16	chr6:165723708-165723758	AG09319	gingival:	n/a
17	chr6:165723708-165723758	HMEC	breast:	n/a
18	chr6:165715757-165715807	HAEpiC	amniotic membrane:	n/a
19	chr6:165723796-165723846	HCF	heart:	n/a
20	chr6:165723034-165723084	HPAEpiC	pulmonary alveolar:	n/a
21	chr6:165715240-165715290	AG10803	skin:	n/a
22	chr6:165715586-165715636	SK-N-SH_RA	brain:	n/a
23	chr6:165723034-165723084	ECC-1	luminal epithelium:	n/a
24	chr6:165724355-165724405	SK-N-MC	brain:	n/a
25	chr6:165722858-165722908	SK-N-SH_RA	brain:	n/a
26	chr6:165715240-165715290	Caco-2	colon:	n/a
27	chr6:165724355-165724405	A549	lung:	n/a
28	chr6:165722651-165722701	NH-A	brain:	n/a
29	chr6:165715240-165715290	AG04450	lung:	fetal
30	chr6:165723034-165723084	GM12878	blood:	n/a
31	chr6:165715757-165715807	HRPEpiC	eye:	n/a
32	chr6:165715592-165715642	NHDF-neo	bronchial:	n/a
33	chr6:165723708-165723758	Caco-2	colon:	n/a
34	chr6:165724355-165724405	IMR90	lung:	fetal
35	chr6:165724355-165724405	ProgFib	skin:	n/a
36	chr6:165715757-165715807	NT2-D1	testis:	n/a
37	chr6:165715757-165715807	HRE	kidney:	n/a
38	chr6:165715240-165715290	ProgFib	skin:	n/a
39	chr6:165722651-165722701	HEK293	kidney:	embryo
40	chr6:165723796-165723846	RPTEC	kidney:	n/a
41	chr6:165723708-165723758	AoSMC	blood vessel:	n/a
42	chr6:165722858-165722908	HepG2	liver:	n/a
43	chr6:165722858-165722908	NT2-D1	testis:	n/a
44	chr6:165723708-165723758	GM12878	blood:	n/a
45	chr6:165722651-165722701	SK-N-MC	brain:	n/a
46	chr6:165722651-165722701	HRPEpiC	eye:	n/a
47	chr6:165715586-165715636	HUVEC	blood vessel:	n/a
48	chr6:165715592-165715642	HUVEC	blood vessel:	n/a
49	chr6:165715592-165715642	GM06990	blood:	n/a
50	chr6:165715757-165715807	Caco-2	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:165726694..165728455-chr6:165728585..165730141,2	MCF-7	breast:
2	chr6:165726694..165728455-chr6:165728585..165730141,2	MCF-7	breast:

No data

Variant related genes	Relation type
C6orf118	TF binding region
C6orf118	CpG island

Extended variants
information (count: 532 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs143689124	chr6:165715101-165715102	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs199773031	chr6:165715121-165715122	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533114758	chr6:165715126-165715127	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs146831067	chr6:165715131-165715132	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs551601424	chr6:165715137-165715138	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs140500230	chr6:165715153-165715154	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs201539458	chr6:165715177-165715178	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376435891	chr6:165715189-165715190	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369703297	chr6:165715190-165715191	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373472563	chr6:165715203-165715204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs376679255	chr6:165715205-165715206	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs371284693	chr6:165715207-165715208	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs534069105	chr6:165715211-165715212	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs200552833	chr6:165715219-165715220	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs145574207	chr6:165715271-165715272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs545305011	chr6:165715296-165715297	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368120575	chr6:165715297-165715298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs36007498	chr6:165715314-165715315	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs372817604	chr6:165715334-165715335	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs199710080	chr6:165715342-165715343	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377236792	chr6:165715344-165715345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35713301	chr6:165715359-165715360	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs572724396	chr6:165715373-165715374	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs267600889	chr6:165715382-165715383	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs202048007	chr6:165715430-165715431	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34717417	chr6:165715433-165715434	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142001393	chr6:165715441-165715442	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145866024	chr6:165715443-165715444	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs370196350	chr6:165715449-165715450	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs9459355	chr6:165715460-165715461	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs141207584	chr6:165715463-165715464	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs150870882	chr6:165715464-165715465	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138289053	chr6:165715467-165715468	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11553361	chr6:165715481-165715482	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs149637046	chr6:165715503-165715504	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568427910	chr6:165715512-165715513	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146166260	chr6:165715517-165715518	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140022567	chr6:165715540-165715541	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200236975	chr6:165715541-165715542	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs143539145	chr6:165715542-165715543	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374675192	chr6:165715543-165715544	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs146305345	chr6:165715556-165715557	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs367717621	chr6:165715557-165715558	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200810534	chr6:165715558-165715559	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs41268587	chr6:165715574-165715575	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs576752319	chr6:165715578-165715579	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs376226266	chr6:165715597-165715598	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200166060	chr6:165715602-165715603	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs543835994	chr6:165715610-165715611	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs372557658	chr6:165715622-165715623	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Ovarian cancer	21720365	CNVD
Glioblastoma multiforme	21138945	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:227 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165713600-165715800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:165714400-165715600	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:165714400-165721800	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:165714600-165715200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:165714600-165715400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:165714600-165716200	Strong transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:165714600-165721200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr6:165714800-165715600	Strong transcription	Fetal Brain Female	brain
9	chr6:165714800-165721600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:165715200-165716200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr6:165715400-165715800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:165715600-165716000	Weak transcription	Fetal Brain Female	brain
13	chr6:165715600-165720400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:165715800-165716200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr6:165716200-165716800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
16	chr6:165716200-165716800	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr6:165716800-165721200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr6:165716800-165721400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr6:165721200-165721400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr6:165721200-165721400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr6:165721200-165721400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr6:165721200-165721800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr6:165721400-165721600	Enhancers	Gastric	stomach
24	chr6:165721400-165721800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr6:165721400-165721800	Active TSS	Brain Germinal Matrix	brain
26	chr6:165721400-165722200	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr6:165721400-165722600	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:165721400-165722600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr6:165721400-165723200	Active TSS	Brain Anterior Caudate	brain
30	chr6:165721600-165722600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:165721600-165722800	Weak transcription	Gastric	stomach
32	chr6:165721800-165722000	Active TSS	Skeletal Muscle Female	skeletal muscle
33	chr6:165721800-165722200	Enhancers	Esophagus	oesophagus
34	chr6:165721800-165722400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr6:165721800-165722400	Flanking Active TSS	Brain Germinal Matrix	brain
36	chr6:165721800-165722400	Enhancers	Fetal Muscle Leg	muscle
37	chr6:165721800-165722600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr6:165722000-165722200	Enhancers	Fetal Brain Female	brain
39	chr6:165722200-165722400	Enhancers	Breast Myoepithelial Primary Cells	Breast
40	chr6:165722200-165722400	Active TSS	Primary hematopoietic stem cells	blood
41	chr6:165722200-165722400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr6:165722200-165722400	Enhancers	Brain Substantia Nigra	brain
43	chr6:165722200-165722400	Enhancers	Duodenum Mucosa	Duodenum
44	chr6:165722200-165722400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
45	chr6:165722200-165722400	Active TSS	Fetal Brain Male	brain
46	chr6:165722200-165722400	Enhancers	Fetal Kidney	kidney
47	chr6:165722200-165722400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
48	chr6:165722200-165722400	Enhancers	NH-A	brain
49	chr6:165722200-165722600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:165722200-165722600	Weak transcription	Esophagus	oesophagus

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