Variant report

Variant	nsv970081
Chromosome Location	chr6:26037423-26044104
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:288)
CpG islands
(count:306)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:26043893-26044837	HepG2	liver:	n/a	n/a
2	ATF2	chr6:26043700-26044766	GM12878	blood:	n/a	n/a
3	ATF2	chr6:26043497-26044687	GM12878	blood:	n/a	n/a
4	BCLAF1	chr6:26043256-26043952	GM12878	blood:	n/a	chr6:26043387-26043396
5	BCLAF1	chr6:26043220-26046641	GM12878	blood:	n/a	chr6:26043387-26043396
6	BCLAF1	chr6:26044032-26044800	GM12878	blood:	n/a	n/a
7	BRCA1	chr6:26043898-26044577	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr6:26043848-26044658	HepG2	liver:	n/a	n/a
9	CBX3	chr6:26044069-26044362	K562	blood:	n/a	n/a
10	CEBPB	chr6:26039917-26040077	A549	lung:	n/a	chr6:26039988-26039999
11	CEBPB	chr6:26039840-26040172	HepG2	liver:	n/a	chr6:26039988-26039999
12	CEBPB	chr6:26044030-26044679	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:26043930-26044297	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr6:26039898-26040074	IMR90	lung:	n/a	chr6:26039988-26039999
15	CEBPB	chr6:26039953-26040040	K562	blood:	n/a	chr6:26039988-26039999
16	CEBPB	chr6:26043552-26045220	GM12878	blood:	n/a	n/a
17	CEBPD	chr6:26043204-26044020	HepG2	liver:	n/a	n/a
18	CHD1	chr6:26043294-26046507	GM12878	blood:	n/a	n/a
19	CHD2	chr6:26043933-26044717	HepG2	liver:	n/a	n/a
20	CHD2	chr6:26043866-26044490	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr6:26043594-26044946	GM12878	blood:	n/a	n/a
22	CREB1	chr6:26043378-26046791	HepG2	liver:	n/a	n/a
23	CREB1	chr6:26043258-26046731	HepG2	liver:	n/a	n/a
24	CREB1	chr6:26043748-26044811	GM12878	blood:	n/a	n/a
25	CTCF	chr6:26043720-26043870	HCPEpiC	choroid plexus:	n/a	n/a
26	CTCF	chr6:26043820-26043970	GM12873	blood:	n/a	n/a
27	CTCF	chr6:26043420-26043570	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr6:26041665-26041711	Fibrobl	skin:	n/a	n/a
29	CTCF	chr6:26043366-26043414	GM12878	blood:	n/a	n/a
30	CTCF	chr6:26043560-26043710	SAEC	small airway:	n/a	n/a
31	EBF1	chr6:26043839-26044374	GM12878	blood:	n/a	n/a
32	ELF1	chr6:26044044-26044863	HepG2	liver:	n/a	n/a
33	ELK1	chr6:26044010-26044458	Hela-S3	cervix:	n/a	n/a
34	EP300	chr6:26043582-26044740	SK-N-SH	brain:	n/a	n/a
35	EP300	chr6:26043807-26044708	HepG2	liver:	n/a	n/a
36	ETS1	chr6:26043415-26044017	GM12878	blood:	n/a	n/a
37	FOS	chr6:26043943-26044282	Hela-S3	cervix:	n/a	chr6:26044009-26044018
38	FOS	chr6:26044011-26044249	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr6:26043833-26044294	GM12878	blood:	n/a	chr6:26044009-26044018
40	FOXA1	chr6:26043600-26044887	HepG2	liver:	n/a	n/a
41	FOXA1	chr6:26044047-26045048	HepG2	liver:	n/a	n/a
42	FOXA2	chr6:26043412-26044969	HepG2	liver:	n/a	n/a
43	FOXM1	chr6:26043490-26045092	GM12878	blood:	n/a	n/a
44	FOXM1	chr6:26043504-26044705	GM12878	blood:	n/a	n/a
45	GATA1	chr6:26043395-26046388	PBDE	blood:	n/a	chr6:26045414-26045431
46	GATA3	chr6:26043922-26044720	A549	lung:	n/a	n/a
47	GTF2F1	chr6:26043748-26044372	Hela-S3	cervix:	n/a	chr6:26044205-26044216
48	HEY1	chr6:26043450-26043938	K562	blood:	n/a	n/a
49	HEY1	chr6:26042674-26043060	HepG2	liver:	n/a	n/a
50	HEY1	chr6:26043122-26046696	HepG2	liver:	n/a	n/a

(count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:26043732-26043782	GM06990	blood:	n/a
2	chr6:26043732-26043782	GM06990	blood:	n/a
3	chr6:26043587-26043637	Hela-S3	cervix:	n/a
4	chr6:26043732-26043782	BJ	skin:	n/a
5	chr6:26043546-26043596	U87	brain:	n/a
6	chr6:26043732-26043782	RPTEC	kidney:	n/a
7	chr6:26043732-26043782	PFSK-1	brain:	n/a
8	chr6:26043546-26043596	SKMC	muscle:	n/a
9	chr6:26043587-26043637	HepG2	liver:	n/a
10	chr6:26043820-26043870	AG09309	skin:	n/a
11	chr6:26043820-26043870	SK-N-SH_RA	brain:	n/a
12	chr6:26043546-26043596	PANC-1	pancreas:	n/a
13	chr6:26043732-26043782	HNPCEpiC	eye:	n/a
14	chr6:26043587-26043637	HRCEpiC	kidney:	n/a
15	chr6:26043820-26043870	HL-60	blood:	n/a
16	chr6:26043546-26043596	PrEC	prostate:	n/a
17	chr6:26043990-26044040	HMEC	breast:	n/a
18	chr6:26043732-26043782	MCF-7	breast:	n/a
19	chr6:26043587-26043637	AoSMC	blood vessel:	n/a
20	chr6:26043820-26043870	HUVEC	blood vessel:	n/a
21	chr6:26043820-26043870	SKMC	muscle:	n/a
22	chr6:26043587-26043637	SAEC	small airway:	n/a
23	chr6:26043820-26043870	GM12878	blood:	n/a
24	chr6:26043820-26043870	HCT-116	colon:	n/a
25	chr6:26043732-26043782	NHBE	bronchial:	n/a
26	chr6:26043587-26043637	NB4	blood:	n/a
27	chr6:26043732-26043782	AG04450	lung:	fetal
28	chr6:26043587-26043637	H1-hESC	embryonic stem cell:	embryo
29	chr6:26043990-26044040	U87	brain:	n/a
30	chr6:26043990-26044040	SK-N-SH_RA	brain:	n/a
31	chr6:26043732-26043782	T-47D	breast:	n/a
32	chr6:26043990-26044040	HRE	kidney:	n/a
33	chr6:26043546-26043596	HNPCEpiC	eye:	n/a
34	chr6:26043587-26043637	CMK	blood:	n/a
35	chr6:26043732-26043782	SK-N-MC	brain:	n/a
36	chr6:26043546-26043596	AG09319	gingival:	n/a
37	chr6:26043990-26044040	ProgFib	skin:	n/a
38	chr6:26043820-26043870	IMR90	lung:	fetal
39	chr6:26043546-26043596	SK-N-SH_RA	brain:	n/a
40	chr6:26043587-26043637	SK-N-SH_RA	brain:	n/a
41	chr6:26043546-26043596	HepG2	liver:	n/a
42	chr6:26043820-26043870	HIPEpiC	eye:	n/a
43	chr6:26043587-26043637	HRE	kidney:	n/a
44	chr6:26043587-26043637	LNCaP	prostate:	n/a
45	chr6:26043990-26044040	PANC-1	pancreas:	n/a
46	chr6:26043546-26043596	HCT-116	colon:	n/a
47	chr6:26043820-26043870	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:26043820-26043870	CMK	blood:	n/a
49	chr6:26043587-26043637	HRPEpiC	eye:	n/a
50	chr6:26043990-26044040	AG09319	gingival:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:26033333..26034270-chr6:26043612..26044453,2	NB4	blood:
2	chr2:173420176..173421056-chr6:26043358..26044247,2	Hela-S3	cervix:
3	chr11:68038830..68039554-chr6:26043574..26044468,2	Hela-S3	cervix:
4	chr6:26044049..26046588-chr6:26248373..26251129,2	MCF-7	breast:
5	chr6:26041361..26043937-chr6:26197910..26199861,2	MCF-7	breast:
6	chr3:47555015..47555611-chr6:26043294..26044022,2	Hela-S3	cervix:
7	chr6:26044090..26046416-chr6:26198004..26201095,3	MCF-7	breast:
8	chr4:74708135..74709655-chr6:26042014..26043865,4	MCF-7	breast:
9	chr2:234762991..234763952-chr6:26043968..26044562,2	Hela-S3	cervix:
10	chr6:26043799..26044570-chr6:26157902..26158633,2	Hela-S3	cervix:
11	chr15:65903662..65904236-chr6:26043877..26044663,2	Hela-S3	cervix:
12	chr6:26042662..26045122-chr6:26102656..26104697,2	MCF-7	breast:
13	chr12:6798079..6799041-chr6:26043881..26044486,2	Hela-S3	cervix:
14	chr6:26043872..26047495-chr6:26122651..26127553,11	MCF-7	breast:
15	chr6:26043139..26044932-chr6:27781664..27783621,2	MCF-7	breast:
16	chr12:30948128..30948988-chr6:26043445..26044043,2	Hela-S3	cervix:
17	chr2:202897744..202899372-chr6:26042396..26044227,2	MCF-7	breast:
18	chr6:26041051..26050922-chr6:26154916..26161227,19	MCF-7	breast:
19	chr6:26043570..26047536-chr6:26215421..26218540,6	MCF-7	breast:
20	chr6:26043696..26045642-chr8:144951528..144954310,2	MCF-7	breast:
21	chr6:26043394..26044202-chrX:153193168..153193952,2	Hela-S3	cervix:
22	chr15:93425116..93426959-chr6:26041379..26043913,2	MCF-7	breast:
23	chr21:34914803..34915605-chr6:26043838..26044550,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
HIST1H3C	TF binding region
ENSG00000234816	TF binding region
HIST1H2AB	TF binding region
HIST1H2BB	TF binding region
HIST1H3C	CpG island
ENSG00000234816	CpG island
HIST1H2AB	CpG island
HIST1H2BB	CpG island
ENSG00000180573	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000273209	chromatin interactions
ENSG00000171067	chromatin interactions
ENSG00000126746	chromatin interactions
ENSG00000168274	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000155760	chromatin interactions
ENSG00000227184	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000196374	chromatin interactions
ENSG00000197061	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000187990	chromatin interactions
ENSG00000197846	chromatin interactions
ENSG00000235884	chromatin interactions
ENSG00000159140	chromatin interactions
ENSG00000137259	chromatin interactions
ENSG00000074621	chromatin interactions
ENSG00000272888	chromatin interactions
ENSG00000152256	chromatin interactions
ENSG00000173575	chromatin interactions
ENSG00000182611	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000123485	chromatin interactions
ENSG00000163832	chromatin interactions
ENSG00000159131	chromatin interactions
ENSG00000256316	chromatin interactions
ENSG00000089820	chromatin interactions

Extended variants
information (count: 300 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372590502	chr6:26037432-26037433	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs184405971	chr6:26037433-26037434	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs577869421	chr6:26037461-26037462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs138765831	chr6:26037464-26037465	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189301639	chr6:26037476-26037477	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs181917884	chr6:26037502-26037503	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs117264113	chr6:26037505-26037506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs186566371	chr6:26037572-26037573	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs531488370	chr6:26037581-26037582	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs13210041	chr6:26037601-26037602	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs538210323	chr6:26037617-26037618	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs544972050	chr6:26037655-26037656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs140448461	chr6:26037656-26037657	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs189012270	chr6:26037657-26037658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181842057	chr6:26037677-26037678	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs554857507	chr6:26037688-26037689	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574935888	chr6:26037727-26037728	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560429350	chr6:26037749-26037750	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181575497	chr6:26037753-26037754	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs540475772	chr6:26037776-26037777	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34390238	chr6:26037895-26037896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560739884	chr6:26037900-26037901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs145558464	chr6:26037946-26037947	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs138056170	chr6:26037949-26037950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562916727	chr6:26037953-26037954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs79999363	chr6:26038047-26038048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs59306177	chr6:26038142-26038143	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs562042710	chr6:26038164-26038165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529869044	chr6:26038184-26038185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs77251855	chr6:26038222-26038223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs186414873	chr6:26038265-26038266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs566416702	chr6:26038332-26038333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538576147	chr6:26038343-26038344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs551755770	chr6:26038370-26038371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112250280	chr6:26038423-26038424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370984554	chr6:26038494-26038495	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs554603453	chr6:26038618-26038619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35335639	chr6:26038681-26038682	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs76553022	chr6:26038683-26038684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs571116596	chr6:26038716-26038717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs577607377	chr6:26038736-26038737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546560311	chr6:26038770-26038771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532882759	chr6:26038802-26038803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35329223	chr6:26038832-26038833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563183449	chr6:26038875-26038876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs138426646	chr6:26038903-26038904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs541877155	chr6:26038957-26038958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs78691847	chr6:26038969-26038970	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547685485	chr6:26039031-26039032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149245164	chr6:26039056-26039057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:300 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26034400-26048200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:26034600-26041600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr6:26034600-26044400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:26034800-26043400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr6:26035200-26042400	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:26035400-26042600	Weak transcription	Fetal Kidney	kidney
7	chr6:26035600-26038000	Enhancers	Dnd41	blood
8	chr6:26035600-26043200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr6:26035600-26043200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
10	chr6:26035800-26041000	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:26035800-26042800	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:26035800-26043000	Weak transcription	Thymus	Thymus
13	chr6:26036400-26041000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr6:26036400-26043200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr6:26036800-26043200	Weak transcription	Fetal Thymus	thymus
16	chr6:26037200-26037800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr6:26037800-26038000	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr6:26038000-26041000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
19	chr6:26038000-26043200	Weak transcription	Dnd41	blood
20	chr6:26039600-26043400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr6:26040400-26043000	Weak transcription	Fetal Muscle Leg	muscle
22	chr6:26041000-26041600	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:26041000-26041600	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr6:26041000-26041800	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr6:26041600-26041800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:26041600-26043200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
27	chr6:26041600-26043600	Weak transcription	HUES64 Cell Line	embryonic stem cell
28	chr6:26041800-26043200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr6:26041800-26043400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr6:26042000-26043400	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr6:26042400-26042800	Enhancers	Cortex derived primary cultured neurospheres	brain
32	chr6:26042400-26043200	Enhancers	Primary hematopoietic stem cells	blood
33	chr6:26042600-26042800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr6:26042600-26042800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr6:26042600-26043000	Flanking Active TSS	Fetal Kidney	kidney
36	chr6:26042600-26043200	Enhancers	Primary monocytes fromperipheralblood	blood
37	chr6:26042600-26043200	Enhancers	Primary B cells from peripheral blood	blood
38	chr6:26042600-26043200	Enhancers	Primary T helper cells PMA-I stimulated	--
39	chr6:26042600-26043200	Enhancers	Primary T helper cells fromperipheralblood	blood
40	chr6:26042600-26043200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
41	chr6:26042600-26043200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr6:26042600-26043200	Enhancers	Duodenum Mucosa	Duodenum
43	chr6:26042600-26043200	Active TSS	Monocytes-CD14+_RO01746	blood
44	chr6:26042600-26043400	Enhancers	Fetal Brain Male	brain
45	chr6:26042600-26043400	Enhancers	Stomach Mucosa	stomach
46	chr6:26042600-26044400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr6:26042600-26044600	Active TSS	Fetal Brain Female	brain
48	chr6:26042600-26045800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr6:26042800-26043000	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
50	chr6:26042800-26043000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood

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