Variant report

Variant	nsv970669
Chromosome Location	chr6:5783028-5791204
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:50)
CpG islands
(count:184)
Chromatin interactive
region (count:1)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CHD2	chr6:5783485-5783510	HepG2	liver:	n/a	n/a
2	CTCF	chr6:5783880-5784030	MCF-7	breast:	n/a	n/a
3	CTCF	chr6:5787034-5787145	H1-hESC	embryonic stem cell:	n/a	n/a
4	CTCF	chr6:5783840-5783990	HCPEpiC	choroid plexus:	n/a	n/a
5	CTCF	chr6:5783260-5783530	BE2_C	brain:	n/a	n/a
6	CTCF	chr6:5783404-5783443	H1-hESC	embryonic stem cell:	n/a	n/a
7	CTCF	chr6:5783860-5784010	HBMEC	blood vessel:	n/a	n/a
8	CTCF	chr6:5786880-5787030	GM12873	blood:	n/a	n/a
9	CTCF	chr6:5783860-5784010	AG09309	skin:	n/a	n/a
10	CTCF	chr6:5783860-5784010	WERI-Rb-1	eye:	n/a	n/a
11	CTCF	chr6:5783900-5784050	AG04449	skin:	n/a	n/a
12	CTCF	chr6:5783840-5783990	A549	lung:	n/a	n/a
13	CTCF	chr6:5783360-5783510	BJ	skin:	n/a	n/a
14	CTCF	chr6:5783400-5783550	HBMEC	blood vessel:	n/a	n/a
15	CTCF	chr6:5785180-5785330	WERI-Rb-1	eye:	n/a	n/a
16	CTCF	chr6:5783371-5783453	Fibrobl	skin:	n/a	n/a
17	CTCF	chr6:5786920-5787070	GM12866	blood:	n/a	n/a
18	CTCF	chr6:5783320-5783470	WERI-Rb-1	eye:	n/a	n/a
19	CTCF	chr6:5783860-5784010	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr6:5783880-5784030	AG04450	lung:	n/a	n/a
21	CTCF	chr6:5783660-5783810	HepG2	liver:	n/a	n/a
22	CTCF	chr6:5783451-5783454	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr6:5785596-5785666	GM12892	blood:	n/a	n/a
24	CTCF	chr6:5783280-5783430	WERI-Rb-1	eye:	n/a	n/a
25	CTCF	chr6:5783103-5783117	Pancreas_OC	pancreas:	n/a	n/a
26	CTCF	chr6:5783300-5783450	NHLF	lung:	n/a	n/a
27	CTCF	chr6:5783840-5783990	AG04450	lung:	n/a	n/a
28	CTCF	chr6:5783840-5783990	HAc	cerebellar:	n/a	n/a
29	CTCF	chr6:5783366-5783370	Fibrobl	skin:	n/a	n/a
30	CTCF	chr6:5783340-5783490	HAc	cerebellar:	n/a	n/a
31	CTCF	chr6:5783960-5784110	NHLF	lung:	n/a	n/a
32	CTCF	chr6:5783260-5783410	NHEK	skin:	n/a	n/a
33	CTCF	chr6:5783780-5783930	NHEK	skin:	n/a	n/a
34	CTCF	chr6:5783900-5784050	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr6:5783280-5783430	BE2_C	brain:	n/a	n/a
36	E2F6	chr6:5784028-5784167	K562	blood:	n/a	n/a
37	EBF1	chr6:5786871-5787089	GM12878	blood:	n/a	chr6:5786976-5786987
38	EBF1	chr6:5785553-5785825	GM12878	blood:	n/a	chr6:5785704-5785715
39	EBF1	chr6:5785528-5786109	GM12878	blood:	n/a	chr6:5785704-5785715
40	FOXA1	chr6:5784575-5784730	T-47D	breast:	n/a	n/a
41	GATA3	chr6:5783702-5784153	T-47D	breast:	n/a	n/a
42	GATA3	chr6:5783750-5784080	T-47D	breast:	n/a	n/a
43	MAX	chr6:5783930-5784206	K562	blood:	n/a	n/a
44	MYC	chr6:5786287-5786298	K562	blood:	n/a	n/a
45	NFYB	chr6:5786958-5787296	GM12878	blood:	n/a	chr6:5787124-5787139 chr6:5787127-5787137 chr6:5787124-5787139 chr6:5787126-5787139 chr6:5787125-5787139
46	NFYB	chr6:5786753-5787258	K562	blood:	n/a	chr6:5787124-5787139 chr6:5787127-5787137 chr6:5787124-5787139 chr6:5787126-5787139 chr6:5787125-5787139
47	POLR2A	chr6:5786565-5786653	MCF10A-Er-Src	breast:	n/a	n/a
48	SPI1	chr6:5782692-5783085	HL-60	blood:	n/a	chr6:5782820-5782827
49	TEAD4	chr6:5783818-5784171	H1-hESC	embryonic stem cell:	n/a	n/a
50	TEAD4	chr6:5783756-5784195	H1-hESC	embryonic stem cell:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:5784042-5784092	Caco-2	colon:	n/a
2	chr6:5784042-5784092	Caco-2	colon:	n/a
3	chr6:5783863-5783913	SK-N-MC	brain:	n/a
4	chr6:5784042-5784092	HEK293	kidney:	embryo
5	chr6:5784042-5784092	HNPCEpiC	eye:	n/a
6	chr6:5783863-5783913	AG09309	skin:	n/a
7	chr6:5783800-5783850	LNCaP	prostate:	n/a
8	chr6:5783863-5783913	NHBE	bronchial:	n/a
9	chr6:5783800-5783850	HCF	heart:	n/a
10	chr6:5784042-5784092	PFSK-1	brain:	n/a
11	chr6:5784042-5784092	Jurkat	blood:	n/a
12	chr6:5783800-5783850	SK-N-SH_RA	brain:	n/a
13	chr6:5784042-5784092	GM12891	blood:	n/a
14	chr6:5783800-5783850	GM12892	blood:	n/a
15	chr6:5784042-5784092	HEEpiC	esophagus:	n/a
16	chr6:5783863-5783913	BJ	skin:	n/a
17	chr6:5784042-5784092	T-47D	breast:	n/a
18	chr6:5783800-5783850	MCF-7	breast:	n/a
19	chr6:5784042-5784092	AG04449	skin:	fetal
20	chr6:5783800-5783850	GM12878	blood:	n/a
21	chr6:5783800-5783850	AG10803	skin:	n/a
22	chr6:5783863-5783913	NHDF-neo	bronchial:	n/a
23	chr6:5783800-5783850	AG04449	skin:	fetal
24	chr6:5784042-5784092	GM12892	blood:	n/a
25	chr6:5784042-5784092	HMEC	breast:	n/a
26	chr6:5783863-5783913	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:5784042-5784092	HRCEpiC	kidney:	n/a
28	chr6:5783863-5783913	HRE	kidney:	n/a
29	chr6:5783863-5783913	MCF-7	breast:	n/a
30	chr6:5783863-5783913	Caco-2	colon:	n/a
31	chr6:5783800-5783850	BJ	skin:	n/a
32	chr6:5784042-5784092	LNCaP	prostate:	n/a
33	chr6:5783800-5783850	HRE	kidney:	n/a
34	chr6:5783863-5783913	GM12892	blood:	n/a
35	chr6:5783863-5783913	AoSMC	blood vessel:	n/a
36	chr6:5783800-5783850	CMK	blood:	n/a
37	chr6:5783800-5783850	PrEC	prostate:	n/a
38	chr6:5783863-5783913	PrEC	prostate:	n/a
39	chr6:5783800-5783850	PANC-1	pancreas:	n/a
40	chr6:5783800-5783850	HEK293	kidney:	embryo
41	chr6:5783863-5783913	SK-N-SH	brain:	n/a
42	chr6:5784042-5784092	AG09309	skin:	n/a
43	chr6:5784042-5784092	NHBE	bronchial:	n/a
44	chr6:5783800-5783850	HEEpiC	esophagus:	n/a
45	chr6:5783863-5783913	HAEpiC	amniotic membrane:	n/a
46	chr6:5783800-5783850	HNPCEpiC	eye:	n/a
47	chr6:5783863-5783913	HCM	heart:	n/a
48	chr6:5783800-5783850	SK-N-SH	brain:	n/a
49	chr6:5783800-5783850	AoSMC	blood vessel:	n/a
50	chr6:5783800-5783850	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:25557368..25557868-chr6:5783697..5784353,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NRN1-6	chr6:5788579-5788893	NONHSAT107523
2	lnc-NRN1-6	chr6:5788579-5788932	NONHSAT107524

No data

Variant related genes	Relation type
ENSG00000217239	TF binding region
ENSG00000217239	CpG island

Extended variants
information (count: 388 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562596750	chr6:5783028-5783029	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs576773241	chr6:5783036-5783037	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs545192769	chr6:5783066-5783067	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs112260620	chr6:5783078-5783079	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs374759088	chr6:5783110-5783111	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs184587209	chr6:5783111-5783112	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs527327596	chr6:5783115-5783116	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs527598543	chr6:5783135-5783136	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs548839360	chr6:5783148-5783149	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs547353314	chr6:5783151-5783152	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs113194955	chr6:5783181-5783182	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs531721117	chr6:5783182-5783183	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs386696529	chr6:5783184-5783185	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs17145857	chr6:5783185-5783186	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs149773773	chr6:5783227-5783228	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs531298301	chr6:5783255-5783256	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs17141291	chr6:5783258-5783259	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs566246463	chr6:5783260-5783261	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs536975205	chr6:5783310-5783311	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs73364285	chr6:5783311-5783312	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs573598053	chr6:5783330-5783331	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs537845739	chr6:5783342-5783343	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs149124293	chr6:5783366-5783367	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs577680202	chr6:5783375-5783376	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs544745433	chr6:5783393-5783394	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs561526461	chr6:5783446-5783447	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs145928699	chr6:5783447-5783448	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs17145862	chr6:5783536-5783537	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs542551297	chr6:5783571-5783572	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs17141293	chr6:5783598-5783599	Enhancers Genic enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs531456294	chr6:5783623-5783624	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs192710965	chr6:5783633-5783634	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs565098703	chr6:5783648-5783649	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs185066158	chr6:5783681-5783682	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs532658898	chr6:5783702-5783703	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs372300153	chr6:5783705-5783706	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs9392091	chr6:5783709-5783710	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs115252328	chr6:5783719-5783720	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs112737337	chr6:5783765-5783766	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs141205702	chr6:5783768-5783769	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs570681880	chr6:5783789-5783790	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs146950214	chr6:5783793-5783794	Enhancers Weak transcription Genic enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs148012017	chr6:5783863-5783864	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs375536405	chr6:5783917-5783918	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs538656827	chr6:5783931-5783932	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs4960132	chr6:5783967-5783968	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs73364287	chr6:5783983-5783984	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571130314	chr6:5783999-5784000	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs538375895	chr6:5784021-5784022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs112462884	chr6:5784028-5784029	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Developmental delay	19490664	CNVD
Cancer	21183584	CNVD
Multiple Epiphyseal Dysplasia	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Glaucoma	18694899	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Cancer	20164920	CNVD
Colorectal cancer	21297112	CNVD
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
Thoracic aortic aneurysm	21092924	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
small cell lung cancer	20016488	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
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
dysmorphism	22105932	CNVD
psychomotor delay	22105932	CNVD
Ovarian cancer	19193619	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:161 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5753000-5786000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr6:5766000-5783400	Weak transcription	Brain Hippocampus Middle	brain
3	chr6:5766000-5783400	Weak transcription	Right Atrium	heart
4	chr6:5772200-5783200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:5772800-5786800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr6:5774400-5787400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr6:5776400-5786800	Weak transcription	Thymus	Thymus
8	chr6:5779200-5787200	Weak transcription	Primary B cells from cord blood	blood
9	chr6:5779600-5786600	Weak transcription	Primary T cells from cord blood	blood
10	chr6:5781200-5784400	Enhancers	Fetal Muscle Leg	muscle
11	chr6:5781400-5783400	Enhancers	Primary neutrophils fromperipheralblood	blood
12	chr6:5781400-5784200	Enhancers	Fetal Muscle Trunk	muscle
13	chr6:5781600-5783400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
14	chr6:5781600-5788000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr6:5781800-5783400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:5781800-5783800	Enhancers	Left Ventricle	heart
17	chr6:5781800-5786800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr6:5782000-5783400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr6:5782000-5784400	Enhancers	Fetal Intestine Large	intestine
20	chr6:5782200-5783200	Enhancers	Spleen	Spleen
21	chr6:5782200-5784200	Enhancers	Fetal Heart	heart
22	chr6:5782200-5788200	Enhancers	Fetal Thymus	thymus
23	chr6:5782400-5783600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr6:5782400-5783800	Enhancers	H1 Cell Line	embryonic stem cell
25	chr6:5782400-5783800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr6:5782400-5784000	Enhancers	Stomach Mucosa	stomach
27	chr6:5782400-5784200	Enhancers	Right Ventricle	heart
28	chr6:5782400-5785000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr6:5782600-5783200	Enhancers	Primary monocytes fromperipheralblood	blood
30	chr6:5782600-5783200	Enhancers	Primary B cells from peripheral blood	blood
31	chr6:5782600-5783400	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr6:5782600-5783400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
33	chr6:5782600-5783600	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr6:5782600-5783800	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr6:5782600-5784000	Enhancers	Fetal Brain Female	brain
36	chr6:5782600-5784200	Enhancers	Colonic Mucosa	Colon
37	chr6:5782600-5784200	Enhancers	Fetal Brain Male	brain
38	chr6:5782600-5784200	Enhancers	Fetal Intestine Small	intestine
39	chr6:5782600-5787600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:5782800-5783200	Active TSS	Duodenum Mucosa	Duodenum
41	chr6:5782800-5783200	Enhancers	Rectal Mucosa Donor 29	rectum
42	chr6:5782800-5783400	Enhancers	Gastric	stomach
43	chr6:5782800-5783800	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr6:5782800-5783800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr6:5782800-5783800	Enhancers	Brain Germinal Matrix	brain
46	chr6:5782800-5783800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
47	chr6:5782800-5783800	Enhancers	HSMMtube	muscle
48	chr6:5782800-5784200	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr6:5782800-5784200	Weak transcription	Small Intestine	intestine
50	chr6:5782800-5784400	Enhancers	Placenta	Placenta

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