Variant report

Variant	esv1812259
Chromosome Location	chr6:121404112-121451095
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	CBX3	chr6:121445743-121446140	K562	blood:	n/a	n/a
2	CBX3	chr6:121445765-121446095	K562	blood:	n/a	n/a
3	CBX3	chr6:121445754-121446131	HCT-116	colon:	n/a	n/a
4	CEBPB	chr6:121412311-121412632	K562	blood:	n/a	chr6:121412597-121412610
5	CEBPB	chr6:121415242-121415493	IMR90	lung:	n/a	n/a
6	CEBPB	chr6:121439922-121440215	HepG2	liver:	n/a	chr6:121440100-121440111
7	CEBPB	chr6:121440052-121440142	A549	lung:	n/a	chr6:121440100-121440111
8	CTCF	chr6:121434725-121434800	MCF-7	breast:	n/a	n/a
9	CTCF	chr6:121404200-121404227	Lung_OC	lung:	n/a	n/a
10	CTCF	chr6:121434750-121434772	Hela-S3	cervix:	n/a	n/a
11	CUX1	chr6:121408743-121408830	GM12878	blood:	n/a	n/a
12	E2F4	chr6:121426215-121426598	MCF10A-Er-Src	breast:	n/a	n/a
13	EP300	chr6:121428158-121428410	SK-N-SH_RA	brain:	n/a	chr6:121428177-121428185
14	FOS	chr6:121415121-121415439	MCF10A-Er-Src	breast:	n/a	chr6:121415282-121415290 chr6:121415283-121415290 chr6:121415280-121415292 chr6:121415282-121415291 chr6:121415281-121415290
15	FOS	chr6:121415093-121415410	MCF10A-Er-Src	breast:	n/a	chr6:121415282-121415290 chr6:121415283-121415290 chr6:121415280-121415292 chr6:121415282-121415291 chr6:121415281-121415290
16	FOS	chr6:121415114-121415324	MCF10A-Er-Src	breast:	n/a	chr6:121415282-121415290 chr6:121415283-121415290 chr6:121415280-121415292 chr6:121415282-121415291 chr6:121415281-121415290
17	FOS	chr6:121415124-121415435	MCF10A-Er-Src	breast:	n/a	chr6:121415282-121415290 chr6:121415283-121415290 chr6:121415280-121415292 chr6:121415282-121415291 chr6:121415281-121415290
18	FOSL2	chr6:121415012-121415372	SK-N-SH	brain:	n/a	chr6:121415282-121415290 chr6:121415283-121415290 chr6:121415280-121415292 chr6:121415282-121415291 chr6:121415281-121415290
19	HDAC2	chr6:121426812-121427042	H1-hESC	embryonic stem cell:	n/a	n/a
20	IRF1	chr6:121434324-121434345	K562	blood:	n/a	n/a
21	JUN	chr6:121412983-121413116	HepG2	liver:	n/a	chr6:121412988-121413001
22	JUND	chr6:121412945-121413140	HepG2	liver:	n/a	n/a
23	KAP1	chr6:121445479-121446356	K562	blood:	n/a	n/a
24	MAFK	chr6:121416658-121416705	HepG2	liver:	n/a	n/a
25	MAZ	chr6:121447336-121447526	HepG2	liver:	n/a	n/a
26	MYC	chr6:121433305-121433354	H1-hESC	embryonic stem cell:	n/a	n/a
27	POLR2A	chr6:121436124-121436436	H1-neurons	neurons:	n/a	n/a
28	POLR2A	chr6:121431818-121432328	H1-neurons	neurons:	n/a	n/a
29	POLR2A	chr6:121448359-121448505	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr6:121446576-121446629	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr6:121440387-121440482	GM12878	blood:	n/a	n/a
32	POLR2A	chr6:121425169-121425369	MCF10A-Er-Src	breast:	n/a	n/a
33	POLR2A	chr6:121413227-121413243	MCF10A-Er-Src	breast:	n/a	n/a
34	POLR2A	chr6:121408505-121408838	MCF10A-Er-Src	breast:	n/a	n/a
35	POLR2A	chr6:121428487-121428671	MCF10A-Er-Src	breast:	n/a	n/a
36	POLR2A	chr6:121409806-121409832	MCF10A-Er-Src	breast:	n/a	n/a
37	POLR2A	chr6:121429460-121429506	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr6:121412058-121412156	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr6:121409117-121409253	MCF-7	breast:	n/a	n/a
40	POLR2A	chr6:121449368-121449521	MCF10A-Er-Src	breast:	n/a	n/a
41	POLR2A	chr6:121448691-121448696	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr6:121443407-121443571	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr6:121431688-121432417	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr6:121407800-121408145	H1-neurons	neurons:	n/a	n/a
45	REST	chr6:121431791-121432357	H1-neurons	neurons:	n/a	n/a
46	REST	chr6:121431642-121432588	H1-neurons	neurons:	n/a	n/a
47	SETDB1	chr6:121445368-121446147	U2OS	brain:	n/a	n/a
48	SMC3	chr6:121436216-121436219	GM12878	blood:	n/a	n/a
49	SPI1	chr6:121433492-121433890	HL-60	blood:	n/a	n/a
50	SPI1	chr6:121433468-121433884	HL-60	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:121426802-121426852	U87	brain:	n/a
2	chr6:121426802-121426852	AG09309	skin:	n/a
3	chr6:121426802-121426852	HCF	heart:	n/a
4	chr6:121426802-121426852	H1-hESC	embryonic stem cell:	embryo
5	chr6:121426802-121426852	MCF-7	breast:	n/a
6	chr6:121426802-121426852	HepG2	liver:	n/a
7	chr6:121426802-121426852	AG04449	skin:	fetal
8	chr6:121426802-121426852	Jurkat	blood:	n/a
9	chr6:121426802-121426852	SK-N-SH_RA	brain:	n/a
10	chr6:121426802-121426852	Hela-S3	cervix:	n/a
11	chr6:121426802-121426852	PANC-1	pancreas:	n/a
12	chr6:121426802-121426852	SAEC	small airway:	n/a
13	chr6:121426802-121426852	HRPEpiC	eye:	n/a
14	chr6:121426802-121426852	HIPEpiC	eye:	n/a
15	chr6:121426802-121426852	Hepatocyte	liver:	n/a
16	chr6:121426802-121426852	SKMC	muscle:	n/a
17	chr6:121426802-121426852	T-47D	breast:	n/a
18	chr6:121426802-121426852	GM12891	blood:	n/a
19	chr6:121426802-121426852	HEK293	kidney:	embryo
20	chr6:121426802-121426852	Caco-2	colon:	n/a
21	chr6:121426802-121426852	HNPCEpiC	eye:	n/a
22	chr6:121426802-121426852	HCT-116	colon:	n/a
23	chr6:121426802-121426852	AoSMC	blood vessel:	n/a
24	chr6:121426802-121426852	HCPEpiC	choroid plexus:	n/a
25	chr6:121426802-121426852	IMR90	lung:	fetal
26	chr6:121426802-121426852	GM12892	blood:	n/a
27	chr6:121426802-121426852	NT2-D1	testis:	n/a
28	chr6:121426802-121426852	AG04450	lung:	fetal
29	chr6:121426802-121426852	SK-N-MC	brain:	n/a
30	chr6:121426802-121426852	HMEC	breast:	n/a
31	chr6:121426802-121426852	AG09319	gingival:	n/a
32	chr6:121426802-121426852	ProgFib	skin:	n/a
33	chr6:121426802-121426852	K562	blood:	n/a
34	chr6:121426802-121426852	NB4	blood:	n/a
35	chr6:121426802-121426852	BE2_C	brain:	n/a
36	chr6:121426802-121426852	NHDF-neo	bronchial:	n/a
37	chr6:121426802-121426852	HAEpiC	amniotic membrane:	n/a
38	chr6:121426802-121426852	HUVEC	blood vessel:	n/a
39	chr6:121426802-121426852	GM06990	blood:	n/a
40	chr6:121426802-121426852	A549	lung:	n/a
41	chr6:121426802-121426852	CMK	blood:	n/a
42	chr6:121426802-121426852	BJ	skin:	n/a
43	chr6:121426802-121426852	AG10803	skin:	n/a
44	chr6:121426802-121426852	HEEpiC	esophagus:	n/a
45	chr6:121426802-121426852	HCM	heart:	n/a
46	chr6:121426802-121426852	ECC-1	luminal epithelium:	n/a
47	chr6:121426802-121426852	GM19239	blood:	n/a
48	chr6:121426802-121426852	RPTEC	kidney:	n/a
49	chr6:121426802-121426852	NH-A	brain:	n/a
50	chr6:121426802-121426852	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:121447900..121449925-chr6:121452116..121453757,2	K562	blood:
2	chr6:121400057..121403003-chr6:121403745..121405643,2	K562	blood:
3	chr6:121411153..121412968-chr6:121418070..121419760,2	MCF-7	breast:
4	chr6:119886303..119888450-chr6:121450603..121452607,2	K562	blood:
5	chr6:121395589..121397315-chr6:121403904..121405742,2	K562	blood:
6	chr6:121432266..121434727-chr6:121435842..121438416,2	K562	blood:
7	chr6:121412403..121414647-chr6:121418696..121420931,2	K562	blood:
8	chr6:121399181..121401952-chr6:121402264..121404345,2	K562	blood:
9	chr6:121449170..121450755-chr6:121455147..121457619,2	MCF-7	breast:
10	chr6:121411153..121412968-chr6:121418070..121419760,2	MCF-7	breast:
11	chr6:121412403..121414647-chr6:121418696..121420931,2	K562	blood:

Variant related genes	Relation type
TBC1D32	TF binding region
TBC1D32	CpG island
ENSG00000146350	chromatin interactions

Extended variants
information (count: 1695 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:1695 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9401367	chr6:121404112-121404113	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188573911	chr6:121404144-121404145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148663704	chr6:121404160-121404161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs575952325	chr6:121404164-121404165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369815957	chr6:121404208-121404209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs545295603	chr6:121404258-121404259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs192947329	chr6:121404294-121404295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2358137	chr6:121404311-121404312	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs142188006	chr6:121404323-121404324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs561341758	chr6:121404334-121404335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530173462	chr6:121404336-121404337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561970081	chr6:121404353-121404354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201625231	chr6:121404392-121404393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs112427020	chr6:121404396-121404397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs373694801	chr6:121404397-121404398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370736698	chr6:121404398-121404399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs3038149	chr6:121404400-121404401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569985627	chr6:121404421-121404422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs184742927	chr6:121404504-121404505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs140352109	chr6:121404526-121404527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs145583055	chr6:121404534-121404535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs73766691	chr6:121404617-121404618	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs146412418	chr6:121404642-121404643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1776805	chr6:121404652-121404653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs74296971	chr6:121404694-121404695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188017008	chr6:121404723-121404724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs556033502	chr6:121404725-121404726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs113019089	chr6:121404737-121404738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372989205	chr6:121404741-121404742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs575983133	chr6:121404751-121404752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544641220	chr6:121404784-121404785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs558804747	chr6:121404785-121404786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs572374451	chr6:121404815-121404816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs17052877	chr6:121404842-121404843	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs191234437	chr6:121404846-121404847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs530232136	chr6:121404849-121404850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543893253	chr6:121404863-121404864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563671653	chr6:121404894-121404895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556937100	chr6:121404927-121404928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532534837	chr6:121404951-121404952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183766816	chr6:121404958-121404959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573995177	chr6:121404965-121404966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566095362	chr6:121405023-121405024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527541699	chr6:121405035-121405036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144649441	chr6:121405094-121405095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138555811	chr6:121405140-121405141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs56822960	chr6:121405185-121405186	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs188433647	chr6:121405220-121405221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553308721	chr6:121405344-121405345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373586442	chr6:121405354-121405355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Gastric cancer	17908304	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
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Breast cancer	21611746	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Ependymoma	18628472	CNVD
Ewing''s sarcoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:288 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:121390800-121444000	Weak transcription	Ovary	ovary
2	chr6:121403600-121443400	Weak transcription	Left Ventricle	heart
3	chr6:121405800-121432000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr6:121411800-121412600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr6:121411800-121443000	Weak transcription	Primary T cells from cord blood	blood
6	chr6:121412200-121413200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr6:121412400-121412600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr6:121412600-121413200	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr6:121412600-121426200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr6:121413000-121413400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr6:121413000-121413400	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr6:121414400-121414800	Enhancers	Brain Germinal Matrix	brain
13	chr6:121415400-121442200	Weak transcription	Primary hematopoietic stem cells	blood
14	chr6:121418000-121442200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr6:121418200-121436000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr6:121418200-121443800	Weak transcription	Dnd41	blood
17	chr6:121418400-121422600	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr6:121418600-121446200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr6:121418800-121434400	Weak transcription	Fetal Intestine Large	intestine
20	chr6:121419800-121446200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
21	chr6:121425800-121426400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr6:121426000-121426600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr6:121426000-121427000	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr6:121426200-121427000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:121426200-121427200	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr6:121426400-121427200	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr6:121426400-121427200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
28	chr6:121426600-121426800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
29	chr6:121426600-121445200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr6:121426800-121427000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr6:121426800-121427200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr6:121427000-121427200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
33	chr6:121427000-121427600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr6:121427200-121427800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr6:121427200-121427800	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr6:121427600-121427800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr6:121428600-121429800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr6:121429400-121429600	Enhancers	Brain Substantia Nigra	brain
39	chr6:121429600-121455600	Weak transcription	Brain Substantia Nigra	brain
40	chr6:121429800-121434600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:121432000-121434400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
42	chr6:121432600-121444000	Weak transcription	Primary T helper cells fromperipheralblood	blood
43	chr6:121433000-121445200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr6:121433200-121434400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr6:121433800-121446200	Weak transcription	Pancreas	Pancrea
46	chr6:121434400-121442400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr6:121436000-121443000	Weak transcription	Primary B cells from cord blood	blood
48	chr6:121436200-121442400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:121436400-121445600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
50	chr6:121436600-121445400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood

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