Variant report

Variant	nsv5586
Chromosome Location	chr6:165694448-165747217
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:106)
CpG islands
(count:856)
Chromatin interactive
region (count:4)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:106 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:165711237-165711322	K562	blood:	n/a	n/a
2	CBX3	chr6:165734725-165734917	K562	blood:	n/a	n/a
3	CHD2	chr6:165722731-165723055	Hela-S3	cervix:	n/a	n/a
4	CHD2	chr6:165722861-165723245	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr6:165702273-165702305	GM13976	blood:	n/a	n/a
6	CTCF	chr6:165722820-165722970	HCPEpiC	choroid plexus:	n/a	n/a
7	CTCF	chr6:165736740-165736890	GM12875	blood:	n/a	n/a
8	CTCF	chr6:165702312-165702326	GM13976	blood:	n/a	n/a
9	CTCF	chr6:165710060-165710210	GM12871	blood:	n/a	n/a
10	CTCF	chr6:165743720-165743870	GM06990	blood:	n/a	n/a
11	CTCF	chr6:165696944-165696988	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr6:165706878-165706926	ProgFib	skin:	n/a	n/a
13	E2F6	chr6:165722358-165722715	A549	lung:	n/a	chr6:165722645-165722660
14	E2F6	chr6:165705916-165706579	H1-hESC	embryonic stem cell:	n/a	chr6:165706472-165706486
15	E2F6	chr6:165722059-165723307	H1-hESC	embryonic stem cell:	n/a	chr6:165722645-165722660
16	E2F6	chr6:165722203-165723274	H1-hESC	embryonic stem cell:	n/a	chr6:165722645-165722660
17	E2F6	chr6:165706084-165706485	H1-hESC	embryonic stem cell:	n/a	n/a
18	E2F6	chr6:165722373-165722547	K562	blood:	n/a	n/a
19	ELK1	chr6:165722938-165722976	Hela-S3	cervix:	n/a	n/a
20	FOS	chr6:165707958-165708267	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr6:165708014-165708255	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr6:165708023-165708213	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr6:165707946-165708268	MCF10A-Er-Src	breast:	n/a	n/a
24	FOXA2	chr6:165709629-165709857	A549	lung:	n/a	n/a
25	GATA2	chr6:165721218-165721628	SH-SY5Y	brain:	n/a	n/a
26	HA-E2F1	chr6:165722465-165723210	MCF-7	breast:	n/a	chr6:165722645-165722660
27	JUN	chr6:165723053-165723253	H1-hESC	embryonic stem cell:	n/a	n/a
28	JUND	chr6:165722982-165723148	H1-hESC	embryonic stem cell:	n/a	n/a
29	JUND	chr6:165708025-165708225	HepG2	liver:	n/a	chr6:165708102-165708113
30	JUND	chr6:165733281-165733292	K562	blood:	n/a	n/a
31	JUND	chr6:165722959-165723157	H1-hESC	embryonic stem cell:	n/a	n/a
32	KAP1	chr6:165722299-165723318	HEK293	kidney:	n/a	n/a
33	KAP1	chr6:165734682-165735137	U2OS	brain:	n/a	chr6:165734965-165734973
34	KAP1	chr6:165734550-165735482	HEK293	kidney:	n/a	chr6:165734965-165734973
35	KAP1	chr6:165722694-165723255	U2OS	brain:	n/a	n/a
36	MAFK	chr6:165738734-165738880	HepG2	liver:	n/a	n/a
37	MAFK	chr6:165738693-165738846	HepG2	liver:	n/a	n/a
38	MAX	chr6:165706173-165706419	H1-hESC	embryonic stem cell:	n/a	n/a
39	MAX	chr6:165722597-165723090	A549	lung:	n/a	n/a
40	MAX	chr6:165722235-165723305	H1-hESC	embryonic stem cell:	n/a	n/a
41	MAX	chr6:165722435-165722541	A549	lung:	n/a	n/a
42	MAX	chr6:165706233-165706498	H1-hESC	embryonic stem cell:	n/a	n/a
43	MAX	chr6:165706162-165706428	H1-hESC	embryonic stem cell:	n/a	n/a
44	MAX	chr6:165722210-165723123	A549	lung:	n/a	n/a
45	MAX	chr6:165722452-165723119	Hela-S3	cervix:	n/a	n/a
46	MAX	chr6:165722322-165723199	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr6:165722256-165723257	H1-hESC	embryonic stem cell:	n/a	n/a
48	MAZ	chr6:165720108-165720147	HepG2	liver:	n/a	n/a
49	MAZ	chr6:165722769-165722825	Hela-S3	cervix:	n/a	n/a
50	MAZ	chr6:165722656-165723287	IMR90	lung:	n/a	n/a

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:165746952-165747002	HEEpiC	esophagus:	n/a
2	chr6:165723034-165723084	HCF	heart:	n/a
3	chr6:165746952-165747002	HEEpiC	esophagus:	n/a
4	chr6:165723034-165723084	HCF	heart:	n/a
5	chr6:165722858-165722908	U87	brain:	n/a
6	chr6:165714960-165715010	A549	lung:	n/a
7	chr6:165714960-165715010	HAEpiC	amniotic membrane:	n/a
8	chr6:165714794-165714844	MCF10A-Er-Src	breast:	n/a
9	chr6:165715586-165715636	HRE	kidney:	n/a
10	chr6:165746952-165747002	HRE	kidney:	n/a
11	chr6:165723034-165723084	T-47D	breast:	n/a
12	chr6:165723034-165723084	HRPEpiC	eye:	n/a
13	chr6:165714794-165714844	Hepatocyte	liver:	n/a
14	chr6:165714794-165714844	SK-N-SH	brain:	n/a
15	chr6:165715240-165715290	HL-60	blood:	n/a
16	chr6:165723796-165723846	PrEC	prostate:	n/a
17	chr6:165714794-165714844	MCF-7	breast:	n/a
18	chr6:165714960-165715010	NB4	blood:	n/a
19	chr6:165724355-165724405	SK-N-SH_RA	brain:	n/a
20	chr6:165715240-165715290	GM12878	blood:	n/a
21	chr6:165724355-165724405	MCF10A-Er-Src	breast:	n/a
22	chr6:165715592-165715642	H1-hESC	embryonic stem cell:	embryo
23	chr6:165715592-165715642	IMR90	lung:	fetal
24	chr6:165722651-165722701	HMEC	breast:	n/a
25	chr6:165723796-165723846	IMR90	lung:	fetal
26	chr6:165714960-165715010	AoSMC	blood vessel:	n/a
27	chr6:165723796-165723846	AG09309	skin:	n/a
28	chr6:165722651-165722701	Hela-S3	cervix:	n/a
29	chr6:165722858-165722908	AG04449	skin:	fetal
30	chr6:165715757-165715807	NHBE	bronchial:	n/a
31	chr6:165715757-165715807	SK-N-SH	brain:	n/a
32	chr6:165715240-165715290	Caco-2	colon:	n/a
33	chr6:165715592-165715642	NH-A	brain:	n/a
34	chr6:165724355-165724405	HAEpiC	amniotic membrane:	n/a
35	chr6:165722651-165722701	HCPEpiC	choroid plexus:	n/a
36	chr6:165715586-165715636	MCF-7	breast:	n/a
37	chr6:165715757-165715807	U87	brain:	n/a
38	chr6:165715240-165715290	ECC-1	luminal epithelium:	n/a
39	chr6:165747029-165747079	HUVEC	blood vessel:	n/a
40	chr6:165715757-165715807	AG04449	skin:	fetal
41	chr6:165723034-165723084	Hela-S3	cervix:	n/a
42	chr6:165722651-165722701	IMR90	lung:	fetal
43	chr6:165715586-165715636	HRCEpiC	kidney:	n/a
44	chr6:165714794-165714844	IMR90	lung:	fetal
45	chr6:165715757-165715807	HAEpiC	amniotic membrane:	n/a
46	chr6:165723796-165723846	RPTEC	kidney:	n/a
47	chr6:165723708-165723758	RPTEC	kidney:	n/a
48	chr6:165714794-165714844	AG09319	gingival:	n/a
49	chr6:165714794-165714844	LNCaP	prostate:	n/a
50	chr6:165715240-165715290	GM12891	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:165746371..165749114-chr6:165759117..165761315,2	MCF-7	breast:
2	chr6:165726694..165728455-chr6:165728585..165730141,2	MCF-7	breast:
3	chr6:165726694..165728455-chr6:165728585..165730141,2	MCF-7	breast:
4	chr6:165693401..165693973-chr6:165739529..165740029,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf118-3	chr6:165695129-165695511	NONHSAT116001
2	lnc-C6orf118-3	chr6:165694970-165695025	NONHSAT116001
3	lnc-C6orf118-3	chr6:165695129-165695184	NONHSAT116000
4	lnc-C6orf118-3	chr6:165694970-165695025	NONHSAT116000
5	lnc-SDIM1-2	chr6:165740975-165742467	NONHSAT116002

No data

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

Extended variants
information (count: 1910 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1910 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374903735	chr6:165694459-165694460	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs528418693	chr6:165694511-165694512	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs546858906	chr6:165694554-165694555	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs561968753	chr6:165694635-165694636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529277447	chr6:165694665-165694666	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551103480	chr6:165694697-165694698	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569325741	chr6:165694720-165694721	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539935549	chr6:165694755-165694756	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs558537806	chr6:165694810-165694811	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552043736	chr6:165694821-165694822	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567037621	chr6:165694912-165694913	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs36118021	chr6:165694915-165694916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs1333501	chr6:165694945-165694946	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573746844	chr6:165694995-165694996	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
15	rs186722248	chr6:165695011-165695012	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
16	rs544443751	chr6:165695029-165695030	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574361572	chr6:165695039-165695040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2275216	chr6:165695049-165695050	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs113604576	chr6:165695051-165695052	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs112233719	chr6:165695059-165695060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs60637681	chr6:165695061-165695062	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs371373660	chr6:165695082-165695083	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545486250	chr6:165695091-165695092	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80166511	chr6:165695118-165695119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564161427	chr6:165695128-165695129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs572972095	chr6:165695134-165695135	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
27	rs142447513	chr6:165695138-165695139	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs375970650	chr6:165695152-165695153	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs185829884	chr6:165695185-165695186	Weak transcription Strong transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs554455564	chr6:165695269-165695270	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs529308477	chr6:165695271-165695272	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs374758120	chr6:165695318-165695319	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs562859957	chr6:165695377-165695378	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs533497944	chr6:165695415-165695416	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
35	rs77586953	chr6:165695433-165695434	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs113990386	chr6:165695461-165695462	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs375845882	chr6:165695481-165695482	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs188297575	chr6:165695490-165695491	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs139127540	chr6:165695531-165695532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs56203950	chr6:165695553-165695554	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs567576331	chr6:165695632-165695633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538148522	chr6:165695639-165695640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs574460996	chr6:165695661-165695662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556581374	chr6:165695714-165695715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs35401087	chr6:165695722-165695723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs574880496	chr6:165695724-165695725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1333500	chr6:165695812-165695813	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs557807096	chr6:165695814-165695815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs572969006	chr6:165695839-165695840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143722522	chr6:165695885-165695886	Weak 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:345 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:165682800-165696600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:165682800-165714400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:165683400-165696600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:165683400-165696800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr6:165688600-165696600	Weak transcription	Cortex derived primary cultured neurospheres	brain
6	chr6:165692400-165704200	Weak transcription	Fetal Brain Male	brain
7	chr6:165693800-165695200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr6:165695200-165696600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr6:165696400-165696800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:165696600-165696800	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
11	chr6:165696600-165697600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:165696600-165697600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr6:165696600-165698200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:165696800-165697000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr6:165696800-165698000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr6:165696800-165700800	Weak transcription	Cortex derived primary cultured neurospheres	brain
17	chr6:165697000-165698000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr6:165697600-165698000	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:165698000-165698800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:165698000-165701400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr6:165698200-165703000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:165698800-165702000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr6:165700800-165701200	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
24	chr6:165700800-165702200	ZNF genes & repeats	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr6:165701200-165712000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr6:165701400-165703400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:165702000-165707000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr6:165702200-165712000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr6:165702600-165714800	Weak transcription	Fetal Brain Female	brain
30	chr6:165703000-165707200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr6:165703400-165712400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr6:165704000-165714400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr6:165704200-165704400	ZNF genes & repeats	Fetal Brain Male	brain
34	chr6:165704400-165707400	Weak transcription	Fetal Brain Male	brain
35	chr6:165707000-165710000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr6:165707200-165710000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:165710000-165710400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:165710000-165711200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:165710400-165711400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:165711200-165711600	Genic enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:165711400-165713400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:165711600-165713200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:165712000-165712400	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr6:165712000-165713000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr6:165712400-165713000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr6:165712400-165713000	Enhancers	Brain Hippocampus Middle	brain
47	chr6:165712400-165714000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr6:165713000-165713600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr6:165713000-165714000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:165713200-165714600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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