Variant report

Variant	nsv605344
Chromosome Location	chr6:167724650-167778498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:622)
CpG islands
(count:1527)
Chromatin interactive
region (count:11)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:622 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
3	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
4	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
9	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
10	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
11	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
12	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
13	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
14	BHLHE40	chr6:167754879-167756141	HepG2	liver:	n/a	n/a
15	BHLHE40	chr6:167733252-167733970	HepG2	liver:	n/a	n/a
16	BHLHE40	chr6:167732490-167732554	GM12878	blood:	n/a	n/a
17	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
18	BHLHE40	chr6:167755531-167755951	HepG2	liver:	n/a	n/a
19	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
20	BHLHE40	chr6:167764785-167765457	GM12878	blood:	n/a	n/a
21	BHLHE40	chr6:167764869-167765070	K562	blood:	n/a	n/a
22	BRCA1	chr6:167750805-167750846	HepG2	liver:	n/a	n/a
23	BRCA1	chr6:167764922-167765205	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr6:167742236-167742292	K562	blood:	n/a	n/a
25	CEBPB	chr6:167762531-167762769	A549	lung:	n/a	n/a
26	CEBPB	chr6:167762489-167763000	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:167742112-167742401	HepG2	liver:	n/a	n/a
28	CEBPB	chr6:167764886-167765190	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:167778443-167778483	K562	blood:	n/a	n/a
30	CEBPB	chr6:167755617-167756086	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:167755544-167755995	HepG2	liver:	n/a	n/a
32	CEBPD	chr6:167755623-167755941	HepG2	liver:	n/a	n/a
33	CEBPZ	chr6:167755646-167756073	HepG2	liver:	n/a	n/a
34	CHD1	chr6:167765061-167765260	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr6:167764623-167765220	H1-hESC	embryonic stem cell:	n/a	chr6:167764680-167764690
36	CHD2	chr6:167755626-167755922	HepG2	liver:	n/a	n/a
37	CREB1	chr6:167764773-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
38	CREB1	chr6:167755519-167756217	HepG2	liver:	n/a	n/a
39	CREB1	chr6:167762651-167763058	HepG2	liver:	n/a	n/a
40	CREB1	chr6:167755173-167756203	HepG2	liver:	n/a	n/a
41	CTCF	chr6:167764735-167765241	A549	lung:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
42	CTCF	chr6:167764940-167765090	AG04449	skin:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
43	CTCF	chr6:167764920-167765070	AG09319	gingival:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
44	CTCF	chr6:167764940-167765090	HCM	heart:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
45	CTCF	chr6:167764980-167765130	GM12867	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
46	CTCF	chr6:167742631-167742698	GM19240	blood:	n/a	n/a
47	CTCF	chr6:167764909-167765191	GM13977	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
48	CTCF	chr6:167764960-167765110	HepG2	liver:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
49	CTCF	chr6:167765000-167765150	HCT-116	colon:	n/a	chr6:167765037-167765055 chr6:167765039-167765052
50	CTCF	chr6:167764916-167765175	GM10266	blood:	n/a	chr6:167765037-167765055 chr6:167765039-167765052

(count:1527 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167753807-167753857	HPAEpiC	pulmonary alveolar:	n/a
2	chr6:167753807-167753857	LNCaP	prostate:	n/a
3	chr6:167753807-167753857	HPAEpiC	pulmonary alveolar:	n/a
4	chr6:167753807-167753857	LNCaP	prostate:	n/a
5	chr6:167756099-167756149	HCM	heart:	n/a
6	chr6:167727700-167727750	SKMC	muscle:	n/a
7	chr6:167768382-167768432	Jurkat	blood:	n/a
8	chr6:167764620-167764670	SKMC	muscle:	n/a
9	chr6:167764967-167765017	GM12891	blood:	n/a
10	chr6:167765215-167765265	HEEpiC	esophagus:	n/a
11	chr6:167753807-167753857	GM12891	blood:	n/a
12	chr6:167738342-167738392	NHBE	bronchial:	n/a
13	chr6:167738342-167738392	HEK293	kidney:	embryo
14	chr6:167768382-167768432	AG04449	skin:	fetal
15	chr6:167738277-167738327	HRPEpiC	eye:	n/a
16	chr6:167764523-167764573	Caco-2	colon:	n/a
17	chr6:167738425-167738475	Jurkat	blood:	n/a
18	chr6:167734054-167734104	MCF10A-Er-Src	breast:	n/a
19	chr6:167764146-167764196	LNCaP	prostate:	n/a
20	chr6:167764146-167764196	HEK293	kidney:	embryo
21	chr6:167764620-167764670	MCF10A-Er-Src	breast:	n/a
22	chr6:167765215-167765265	SKMC	muscle:	n/a
23	chr6:167765110-167765160	NHBE	bronchial:	n/a
24	chr6:167764146-167764196	PANC-1	pancreas:	n/a
25	chr6:167734054-167734104	GM12878	blood:	n/a
26	chr6:167764523-167764573	GM12891	blood:	n/a
27	chr6:167738425-167738475	SK-N-SH	brain:	n/a
28	chr6:167737937-167737987	HEEpiC	esophagus:	n/a
29	chr6:167739618-167739668	BJ	skin:	n/a
30	chr6:167753807-167753857	GM06990	blood:	n/a
31	chr6:167764146-167764196	PrEC	prostate:	n/a
32	chr6:167738594-167738644	GM19239	blood:	n/a
33	chr6:167764620-167764670	RPTEC	kidney:	n/a
34	chr6:167763758-167763808	NHBE	bronchial:	n/a
35	chr6:167770239-167770289	HRCEpiC	kidney:	n/a
36	chr6:167738425-167738475	HAEpiC	amniotic membrane:	n/a
37	chr6:167738342-167738392	AoSMC	blood vessel:	n/a
38	chr6:167765215-167765265	ProgFib	skin:	n/a
39	chr6:167753807-167753857	AoSMC	blood vessel:	n/a
40	chr6:167739618-167739668	HCM	heart:	n/a
41	chr6:167765215-167765265	IMR90	lung:	fetal
42	chr6:167737937-167737987	NH-A	brain:	n/a
43	chr6:167738425-167738475	SK-N-SH_RA	brain:	n/a
44	chr6:167763975-167764025	HCT-116	colon:	n/a
45	chr6:167761204-167761254	SKMC	muscle:	n/a
46	chr6:167768382-167768432	NH-A	brain:	n/a
47	chr6:167762783-167762833	AG09309	skin:	n/a
48	chr6:167763320-167763370	HUVEC	blood vessel:	n/a
49	chr6:167764146-167764196	H1-hESC	embryonic stem cell:	embryo
50	chr6:167756099-167756149	GM12891	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
2	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
3	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
4	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
5	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
6	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
7	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
8	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
9	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
10	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
11	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
2	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
3	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095

No data

Variant related genes	Relation type
TTLL2	TF binding region
ENSG00000217447	TF binding region
TTLL2	CpG island
ENSG00000217447	CpG island

Extended variants
information (count: 2268 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:2268 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4709165	chr6:167724650-167724651	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536537117	chr6:167724671-167724672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs375905395	chr6:167724680-167724681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369189361	chr6:167724698-167724699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373376704	chr6:167724702-167724703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs371261742	chr6:167724716-167724717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572867681	chr6:167724721-167724722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs543557401	chr6:167724784-167724785	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs12175648	chr6:167724815-167724816	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564941333	chr6:167724879-167724880	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9355626	chr6:167724882-167724883	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs9456265	chr6:167724906-167724907	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs9457297	chr6:167724926-167724927	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs588594	chr6:167724935-167724936	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs112579365	chr6:167724947-167724948	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558901394	chr6:167724965-167724966	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs190710216	chr6:167724981-167724982	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs181809121	chr6:167724982-167724983	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs588981	chr6:167724996-167724997	Enhancers Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186263923	chr6:167725064-167725065	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143175976	chr6:167725066-167725067	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570315005	chr6:167725097-167725098	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552695512	chr6:167725146-167725147	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190589339	chr6:167725194-167725195	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs571007189	chr6:167725234-167725235	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535098364	chr6:167725262-167725263	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9355229	chr6:167725263-167725264	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs181380096	chr6:167725309-167725310	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs389466	chr6:167725321-167725322	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12528753	chr6:167725329-167725330	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs145910742	chr6:167725332-167725333	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185610784	chr6:167725333-167725334	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574079204	chr6:167725354-167725355	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145399466	chr6:167725358-167725359	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs576364908	chr6:167725382-167725383	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112275058	chr6:167725388-167725389	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs35234315	chr6:167725389-167725390	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536985953	chr6:167725391-167725392	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs71553141	chr6:167725392-167725393	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs374218353	chr6:167725398-167725399	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9347194	chr6:167725399-167725400	Enhancers Weak transcription Flanking Active TSS Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs576991369	chr6:167725406-167725407	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs115089969	chr6:167725409-167725410	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558987918	chr6:167725417-167725418	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs66680966	chr6:167725471-167725472	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs639965	chr6:167725529-167725530	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149202722	chr6:167725541-167725542	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs28409153	chr6:167725564-167725565	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562951692	chr6:167725572-167725573	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9347195	chr6:167725574-167725575	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:662 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167720400-167726400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr6:167720400-167727600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr6:167721800-167728000	Enhancers	Fetal Brain Male	brain
4	chr6:167722800-167725000	Enhancers	Liver	Liver
5	chr6:167722800-167727400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr6:167723200-167724800	Enhancers	Stomach Mucosa	stomach
7	chr6:167723400-167724800	Enhancers	Fetal Stomach	stomach
8	chr6:167723600-167725600	Enhancers	Stomach Smooth Muscle	stomach
9	chr6:167723800-167724800	Weak transcription	Rectal Smooth Muscle	rectum
10	chr6:167723800-167724800	Enhancers	A549	lung
11	chr6:167723800-167725200	Enhancers	Colon Smooth Muscle	Colon
12	chr6:167723800-167728400	Enhancers	HepG2	liver
13	chr6:167724000-167725000	Enhancers	Fetal Brain Female	brain
14	chr6:167724200-167724800	Weak transcription	Fetal Intestine Small	intestine
15	chr6:167724200-167725400	Enhancers	Brain Cingulate Gyrus	brain
16	chr6:167724400-167725200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
17	chr6:167724400-167725200	Enhancers	Duodenum Smooth Muscle	Duodenum
18	chr6:167724600-167725200	Enhancers	Brain Angular Gyrus	brain
19	chr6:167724600-167725200	Enhancers	Brain Germinal Matrix	brain
20	chr6:167724600-167725400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:167724600-167725400	Enhancers	Brain Anterior Caudate	brain
22	chr6:167724600-167725600	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr6:167724800-167725200	Enhancers	Cortex derived primary cultured neurospheres	brain
24	chr6:167724800-167725400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr6:167724800-167725400	Enhancers	Rectal Smooth Muscle	rectum
26	chr6:167724800-167726800	Strong transcription	Fetal Intestine Small	intestine
27	chr6:167725000-167725400	Enhancers	Brain Substantia Nigra	brain
28	chr6:167725000-167725400	Flanking Active TSS	Fetal Brain Female	brain
29	chr6:167725200-167726200	Weak transcription	Brain Germinal Matrix	brain
30	chr6:167725200-167730200	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr6:167725400-167726400	Weak transcription	Fetal Brain Female	brain
32	chr6:167725400-167730600	Weak transcription	Rectal Smooth Muscle	rectum
33	chr6:167725600-167726000	Weak transcription	Brain Inferior Temporal Lobe	brain
34	chr6:167726000-167726400	Enhancers	Brain Inferior Temporal Lobe	brain
35	chr6:167726000-167726600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr6:167726200-167726800	Enhancers	Brain Germinal Matrix	brain
37	chr6:167726200-167726800	Enhancers	Placenta Amnion	Placenta Amnion
38	chr6:167726400-167726600	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr6:167726400-167728200	Enhancers	Fetal Brain Female	brain
40	chr6:167726600-167726800	Enhancers	Thymus	Thymus
41	chr6:167726600-167727000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:167726600-167727000	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr6:167726800-167727800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr6:167726800-167728000	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr6:167726800-167730200	Weak transcription	Fetal Intestine Small	intestine
46	chr6:167726800-167730200	Weak transcription	Thymus	Thymus
47	chr6:167727000-167727600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr6:167727000-167727600	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr6:167727000-167728200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:167727200-167727800	Enhancers	HUES48 Cell Line	embryonic stem cell

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