| Tag | Content |
|---|
EnhancerAtlas ID | HS007-14177 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr6:3247680-3249060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr6:3248079-3248090 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr6:3248079-3248090 | GGTGACTCATG | + | 6.02 | | REST | MA0138.2 | chr6:3247715-3247736 | CCCAGCACTCAGGACAGTGCC | + | 6.6 | | TBXT | MA0009.2 | chr6:3248510-3248526 | TCACACATATGTGCAA | - | 6.48 | | TBXT | MA0009.2 | chr6:3248510-3248526 | TCACACATATGTGCAA | + | 6.49 | | ZEB1 | MA0103.3 | chr6:3248162-3248173 | CCCACCTGCCC | + | 6.14 |
|
| | 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 |
| GH06I003246 | chr6 | 3246856 | 3249920 |
|
Enhancer Sequence | GGGGGTCATC GTTCTGAAGG GCATCTTTGT GTCTTCCCAG CACTCAGGAC AGTGCCTGGC 60
ACACAGATGC TTCAGTAAAT GTTTGCCGAG TGAACCCGAT GAATGGGCAT TTTGTCACTG 120
GGTCTTTTCA TTTATTCCTT GGCTTGCTCC CTGTCTCCCC TTGAAACACA GCTGCTTTCA 180
TTGACCGCGT CTTTATTTGT TGGGTGGATG TGCTTGTTTT CAGTGCCAGG AAGGAAAAAC 240
AAGCACAGAA GTCGCCCCTC CCGGGCAGCC ATATTCCCGG CTAAGAAGCC CTCCTTTGTG 300
CCAAGAGCAG AACCGTCTAT GGCTGGGTGG AGGGTCACAG CCTGTGGGAC GGTGCGGAGA 360
GGCAGGGGGG TGCGGCGAGC TCTGGGCTTG CAGGCAGGCG GTGACTCATG CAGAGTCCGG 420
CCACCGGTGC GGGAAAAGGG CTTTGACGTT CTCAGCAAAA CCCCAAGGCG AGCTCCGAGC 480
AGCCCACCTG CCCCTCCCAC CCACGCAGGG CCTTGCAGAT GAATCTGCTT CTGTATCACA 540
TGATCCGTTT CAGCAGGAGA GAGACGGAGA GAAACAGCCT TTTGTTCTGC CAGCCTCCAT 600
GATTGCGTAT CTTAGGCACA ACGCTCTGAA GTCAGGCTGA GGATTCTAAT AAAACTTGGG 660
AAGCTTTACC CGGAAGACAA GGTGCTCTTT CACTAGGCAT GATTTGGACC CAGGATATAA 720
ATTCTCTTTC GTGGGACGGG AGAGTTGTGT CTTTGCTTAT CCTCGGGGAG TCTCACTGTG 780
CCCCACTGAT CATGCGTGCC TTCCAAAGCT GTCAGGTAGC CCCTCCACAA TCACACATAT 840
GTGCAACCAC ATATTTTCCA ACCCAAACGA GGGTACACAC CATCTGGGGA GGGATTCCCC 900
CTTCCCATAT GCGTGAATTC GTTTAGCTAA AAAGCATTAA CAGTCACAAA ATAAAATCAC 960
ATTGAGACCC ACATTTTAAT GGAAACACTG GACCTTTGGG GTTGTGCTGG AGATTTTGAG 1020
ATCTGGGATA AGAAACCCAG AGTGAGCAGG TGGAACAGTT CCCACTGGCT TTGGTGACAT 1080
GGCCCCAGGA CTGCTGTCTA CCTGGAGGGC CTGTTTGGAG CTGATTTCGG AGAGGTGGTG 1140
GCTACACTCC TCGCCACTGT GTGCACGGTG CCTGACCTTG CCTGGAAGCC TGCGTGTTCA 1200
CTTAAATTCA GGTCCTCTGT TCAGCACCCC ATAGCTCCTC ACGGATCCTC ACCCTCCATC 1260
CCTGCCTGGG ATCCCCACTC TTCCACCTGG AAAGGGGTGC AGGGAGGTGG TCCAGGATCC 1320
AAGCCTCAGC TCCACCCTCA GCGACTAAGT GCCTTGTGGG CTCTTCATTT ATTCAGCGTT 1380
|
