| Tag | Content |
|---|
EnhancerAtlas ID | HS053-34285 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr6:43878350-43879360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr6:43878666-43878681 | AGGTCAGCCTGTCCT | + | 7.24 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_14960 | chr6:43876941-43879884 | CD4_Memory_Primary_7pool | | SE_21048 | chr6:43878239-43880149 | CD8_Memory_7pool | | SE_28473 | chr6:43878500-43886662 | Fetal_Intestine | | SE_29305 | chr6:43878259-43886675 | Fetal_Intestine_Large | | SE_39891 | chr6:43878060-43880150 | K562 | | SE_56461 | chr6:43877886-43880040 | u87 | | SE_56790 | chr6:43878606-43879901 | VACO_400 | | SE_65246 | chr6:43878598-43884479 | Pancreatic_islets | | SE_67806 | chr6:43877886-43880040 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I043910 | chr6 | 43878001 | 43886417 |
|
Enhancer Sequence | ACATACAAAT GAATGCACAA ATATACAAAA ACCTACAGTG CAAACATATG CAAGCATATG 60
TGCACATCCA CAGATGCAAA AACTTGCACA AACACATCCA CATTATGTGC ACGAAGAAAC 120
ATGCCCACAT CTGCATGTGT GTGCACACAA TCACGTATGC CTGCCTGGCC TGGTTTATAT 180
GGGGAGTGAT GGAAGAAGGC CATTGGCCTC TCCAGGTTCT GTATGTGTCT GGTGACTTGG 240
AGTGAGTGTG TTTCTTTACT GTTTCCTTGG AGTTGCATCA TAAAGTGCCT TCCTTGAACA 300
GGGCCGGTAC AGGACCAGGT CAGCCTGTCC TCATTACATC AGCAGGGTGA GCCAAGGGAG 360
GTTGCCTAAA AATTCAAGTA AGTAGTCCCC AGCCCATGGA GGCTTGAGAG ACCCCCAAAC 420
CCCTCCCTTT CTCTGGAGTC CCACCTAGGG TTAACCACTG GCTACACTCC CAGGGAGGCC 480
CCAAAAGCTG CCAGATTATG CCCTTTAAGA GATGAGAAAA TGGCTTGACC AAAAAAGTTA 540
ATGTTTGTAA ACACCAGTTT AAGGAGAGAA GGGATTTCAA AGCCTCCGCA GCCTGCTGCT 600
CCACACCTCT GAGCATCTGG GAATCTCAGC CCGGGGCTGT GCACACAGTA GGAGCTACAT 660
CGGCAGCACT CTAGGGAATG GGGTCTGACA AGTGGTGGGG GGTACAGGGA GCCAGCCCCA 720
GAATTCAGAG GTAATGCAGA CCCTCTTCAC GTTTGAGGAC CCTGCCTGCA TCACTTCCAG 780
CCCAGAGGTT CTTAGCTTCG TCATCTGCTG GGGGTGAGGG ACCACCAGTT TAGGGAGCCC 840
CCTGCAGAGG CCCCCTGGAT TGTCCCTTCT TTTCCCTCCT TGGCCTTCCT CCCAGCTTGG 900
TCTCCCCACC ACCCCCAACA CTCCCCAGAC ACATTCCTCT CCTTCAGACT TTCGTTTCAA 960
GGGCTTGGTG ATTTCTTTGC AGGATTTGAT TTGCCGCTCA GGCATTTCCT 1010
|
