| Tag | Content |
|---|
EnhancerAtlas ID | HS007-07764 | Organism | Homo sapiens | Tissue/cell | BE2C | Coordinate | chr18:57184450-57185820 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr18:57185197-57185218 | GTCACTGTCCGTGGTTCTGAA | - | 8.49 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH18I059515 | chr18 | 57182442 | 57184610 | | GH18I059517 | chr18 | 57185141 | 57185239 |
| Enhancer Sequence | AAAAAGAAGC TAAGAACAGG GCATCAAACT GGCTTTTATT GATTCACCCA TGAACAAGTT 60
GTGCCTTTAC ACTGTTGTTA TTTGTAAGGA ATCCTGGGTA TTTGGCATTC CTGGAATATT 120
CTATTTAGCT ACCTTGGGGT CCAAGTTCCC TTTAACTGGG GGAGAAGAAC TTTTCACCTG 180
TTTCTATGCA TGCTCACAAG GATAAGCCTC CATGATGGCA ATTTTGGCTC TGTTTCAGAT 240
AAAAATTCAT TTAGTAACAT ATAAAGGATA TCAAGTCATG AAGGCACTAC ATAAATGTAA 300
GTACAGCTTA AGCCAGAGCT CACTGACTCT CCATCTCATT TTCATCTGCC AGCATCATTG 360
GACCCGAAGT CATATGGAAG CCACATTTTA AGCCTAAGGG TGTCTAAATT GATTTGACAA 420
AGCCATCAGT CAGTTCTATC CCTTTCTTCC TAGACTCATT TATAAGCACC ACTTAAAACC 480
AGATGCCACT AGCAGTGAGG ACACAAAGCA GCAAGTTTTC AGAGCACCGA GTTTCTCCAC 540
TGGCCATTAG CAGTTAGGCT GGAAGGGGGT TCAGAGCCAC AACTACTGAA AGTCTCACTC 600
CTTGAGTTTG GAAGAGATAA TGAACATTTT CCTGAACATT CAACAAACAT GGTCAAGGGG 660
GCTGGGGATT CCCAAGATCA AAAGAGGGAT CTGTCACAAG ATCATTATGT CCAGAATTGT 720
TGGGCACAGG GGTGTGCTGT CTCCTATGTC ACTGTCCGTG GTTCTGAACC CAGCTGGGCA 780
ATTCTCTGGG AAGTTGGGGG CGGAGGAAAC TTGCACCCAT TCCTAGGCCC TTGGTGAGTG 840
TCCTGAGAAA GAAGGAGATG ATACATTGTG GACTGGGGCA TAAAACAGTG TTAATCAACA 900
CTTTGTTTCC ACCCCCATAG CAGGCACAGT ATTCAGTCAG TTTTTACACA CATTTTGATG 960
TTAAAGTAAT GATTAAGAGA ACAAAGCTGG CTGGGCACAG TGGCTCACTC CTGTAATCCC 1020
AACACTCTGG GAGGCCGAGG CTGGCAGATC ACTTGAAGTT AGGAGTTCAA GACCAGCCTG 1080
GCCAACCTGG TGAAACCCCA TCTCTACTAA AATTACAAAA ATTAGCCGGG TGTGACGACG 1140
CACGTGCCTG TAATTCTAGC TACTTGGGAG GCTGTGGCCG AAGGATCACT TGAACTTGGG 1200
AGGCAGAGGT TGCAGTGAGC CAAGAACAAG CCATTCATAA AATAACTATA AACAGAATTC 1260
TAAATCAATT GTTTGTTAAT GGATCTTCTC TTGTCATCAT ATTCACTGCT GTCTTCAGCT 1320
ATAACTCATG TTGGCTGTAT GTTAAACTTG GCTATTTTCT AATCAGTGGG 1370
|
| |
|
|
|
