| Tag | Content |
|---|
EnhancerAtlas ID | HS177-14493 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr22:29475280-29476460 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr22:29476187-29476205 | CAATCCTTCCCTCCCTCC | - | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr22:29476183-29476201 | CCTTCAATCCTTCCCTCC | - | 6.55 | | TBX20 | MA0689.1 | chr22:29475737-29475748 | CTTCACACCTT | - | 6.32 | | TBX21 | MA0690.1 | chr22:29475738-29475748 | TTCACACCTT | - | 6.02 | | TCF7L2 | MA0523.1 | chr22:29475973-29475987 | TTTCTTTGATGTTC | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_33639 | chr22:29472764-29479401 | H2171 |
|
| | 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 |
| GH22I029077 | chr22 | 29473265 | 29476899 |
|
Enhancer Sequence | AATTGGGGTG CTAGGGAGCA CCTTGGCAGA CAAAATGTTT TAGGCCACCT CACACGCAAA 60
GTTGCCTCTC TCCCTGCATT TATACAACAG GGCCCTCTCA GAGCTACCCC TCTGCCGGGC 120
CCAGCTTCTA GCTTCCCTTG CCACGGATTT AATCTCTGGC AAGTAGCCAA AGCATTAAAC 180
TTTTATTGTT CAATTTGCCA CAAGGGCGGG GCCCTGCTTC TAGTGGGCTG AGGAGGCTGC 240
AGCTGCTTCC AAACCCAAGT GTCACACCAC ATTAGCAACT GCAGACTTTG AGGGCTGGAT 300
TTCTTTCAGT TTGGTTAGAT TCTTGGTTAG AACCAGAACG GTATACTCAC ACACAAAATT 360
TTAAAGCTAG GAAATAGTAA AAACAGTGTA GGCAACTTTT AAAGGTGATT CAGAGCGGCT 420
GTAGCTATCA GCGTGTATGA TTGACTCTGC GTGGTTTCTT CACACCTTCC AAACAGACAT 480
ATTAGATGGC TGTACATGTG CCTTAGTGTC CTAAAGTTGG AGGAAAACAT GGCAACCAAG 540
TAGTTCTCTT CTAGACTAGT AGGGATTGCT AACCAATCCC ATCACAGTAT GTAAATTACT 600
TGCTGTTGTT CAATCTATAA AAATTCATCT TCAAAGAAAA TTATTGGGCT GGTAAAAATA 660
TTTTTAATAA TGACCACAGA AGCCATATTT GTTTTTCTTT GATGTTCTTC CGAAGACCCT 720
TCTGGTTCTA ATCAGATTGT TCCCACATAA AATACAGTGG AAATCTACAA TAATAAAATC 780
CCTATTCCTA TGTCTATGGG GAAATAAACA GGATGGGGAC TGTCCTTTTA AGGGGCTTTC 840
CCCTTCCCTT TCCCCAGACT CAAAGCCTCT ATTACTGGTG GGTGTTTTGG CATCAGTTAA 900
GGGCCTTCAA TCCTTCCCTC CCTCCATGTT TTGCTCTTTC ATTAAAGTGT TTCTGTTGTC 960
TAATTATATC CTTTCAATCA AATTAGAGAC TGTAGCATCT GGTGAGGGCT GTAACTGCTG 1020
CCATCTGCAC CTCGTCTATA CAGGCCTTTT CAGCTGAGAA TCACTCAACT TCCAAATGGC 1080
AGGAAGAGAT TTGGAAAAAG TTTAGTTGGA GGGGAGATTA ACTTAAAAGG AGTGTCTTCA 1140
AAGGCTGGGT GCGATGCCCT GCTTGCTGTG ATGTGTGCAT 1180
|
