| Tag | Content |
|---|
EnhancerAtlas ID | HS037-13983 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr16:24146850-24148300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr16:24147267-24147278 | TTAATCCTCTT | - | 6.14 | | Mecom | MA0029.1 | chr16:24147566-24147580 | AAGACAAGATAAGG | + | 6.61 | | OLIG2 | MA0678.1 | chr16:24147202-24147212 | ACCATATGGT | + | 6.02 | | OLIG2 | MA0678.1 | chr16:24147202-24147212 | ACCATATGGT | - | 6.02 | | Stat6 | MA0520.1 | chr16:24147273-24147288 | CTCTTCCAGAGAACC | + | 6.39 |
|
| | 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 |
| GH16I024135 | chr16 | 24146721 | 24148024 |
|
Enhancer Sequence | CTCGAACTCC TGGCCTCAAG TGATCCGCCT GCCTCAGCCT CCCAAAGTGA TGGGATTACA 60
GGCTTGAGCC ACCACACCTG GCCTCACAGC ATCATCTGCT GGAGCCAAGC CCGGCACCAG 120
ATTTTAACAG GAAGAAATTG CCTGAGGAGA TTAAAAGGCA GCTTAGTTCA TGCCAGGAAC 180
AAAGGCCTTC TCTAAAGTCT GAGCTTCTGT TGTGGGAGTC TCTACTAATT TTAATCTCAT 240
TAGTGGTATG TATTCACACA CAGACATATA CATACATACA TTAGATGTGG TTATATAATC 300
CTACAGACAA AAGCACTTCC CTGTACTTCA GCCTGCTTTG CTATCTTCCT GCACCATATG 360
GTGAGTTCCT TTATCATATG GTTCACAGAT AGCTCAAAGT GTTTGCTACC TGTTTCCTTA 420
ATCCTCTTCC AGAGAACCTT TTTGACATTT GCTGTCTGAT CTTGGATTCC TGCCTTCTCT 480
TTGGTTCTAT CGCAATTATG TCACTTCCCT GCCCCCACCA AGCCTTCAAC CTTTCCTTCT 540
TTCATATGCA ATTCTGATTG CAGCGTGTTT TTTTTTTTTT TTTTGCCAAC TCATCTTCCC 600
AGATCCTCGT GAGGCCCTTC TTCCACCTTC CCGAATTTTC CAGGTCTCTC CTCAATGAAG 660
TGACTTACTG CTCTTCCGCA GCCTCTGCCT TCAATTCTCA GAAGGTAGTA TGTTACAAGA 720
CAAGATAAGG TTCATTTTTC TCAAGAAAAT AAATTATATC AAGGAAAATG AAATGTCAGG 780
AATTTAAGTT TTACAACCTT CCATCTGCTG CAAGTAGATT GTCAAGCCAG AGTGAGTAAA 840
GCGGGTATTT GCTGAGAAGA CATGGCTTGT TTCTGTGTAT CTCAAGACAC CCAGAGGCAA 900
GAAGTGCCAC CTGAATGAGA GAGCTTCCAG CAGTCTGATA ACCATGGCTC CATCTGGGGG 960
GTTGTAGGGG GGCCCCCAGC CTGTCATCCC TGCTTCTCGA TGACATCTCT CTGCAGATAC 1020
GCATCAGCAC CACCTCTCTC AGCCTTGTTG ATGCTTCTCA AGTCTCCATG TCTAATTCTC 1080
ACATGTAGAA TATCCTAGGA ATCTAAAATC CCGGGAAAGA AAAACTGATG GGCCAGTGTG 1140
GACCAGGGAT CCCTAGGATC CAATTCACTG TGACCGGGGA AGCGGTTACT TTTCCAACCA 1200
TCCATCAGGA AAGATGACAA GAAAAGCAAA TAGGATGTGG GCAGTTTTCC TATGAGAAAG 1260
AAGAAAACGA CGGGCCTGTC TGGCACACAG GCCAAAGTGG GAGTTTCCTT TAAATGTGTA 1320
TTATTTTTTA TTTTAATTTT TTTATTTTGT TTATTTATTT ATTTTTGAGA TGGAGTCTCA 1380
CTCTGTCGCC CAGGCTGGAT TGCAGTAGCA TGATCTCGGC TCACTGCAAC CTCCACCTCC 1440
TGGGTTCAAG 1450
|
