| Tag | Content |
|---|
EnhancerAtlas ID | HS176-02715 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr1:170230690-170231940 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2B | MA0660.1 | chr1:170231798-170231810 | ACTATTTATAGT | - | 6.04 | | STAT1 | MA0137.3 | chr1:170231674-170231685 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr1:170231671-170231685 | CCTTTTCCTGGAAA | - | 6.91 | | TEAD1 | MA0090.2 | chr1:170231218-170231228 | ATGGAATGTG | - | 6.02 | | ZNF263 | MA0528.1 | chr1:170231244-170231265 | GGAGGAGAAAAGAGGGAGAGG | + | 6.48 | | ZNF263 | MA0528.1 | chr1:170231241-170231262 | GGGGGAGGAGAAAAGAGGGAG | + | 6.55 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 170231745 | 170231854 | | chr1 | 170231660 | 170231727 |
| Enhancer Sequence | CAATAGAATA AATCCAAACT TGCTTAGAAG TGTGAAGTTC TGGCAGGAGT TAGTAAGATT 60
AGCTAGTTGA CTTTAGCTTT CCTAATCTAA TCCTATGATT GATTTTGATA GAAAAAGAAA 120
GTAACAGACA GGATACCCAG GAGCAGGCTC AAAGTCACCA GTACCTAACA CCGTGAAGTT 180
TTAGTCTGTG TTGACGTAAC TTCAGAGCAC AGTTTTGTAC ACGGAAGAGT TTAAAACATC 240
TCGGGAACAG ATGTAAAGGA ACTCTTCATT TTTAGCAAGA AATGTGGTTA CTGTTGGCCA 300
CCACAGTCAG AACCAGAGGA CACCATGCTG GCTAATGGAA ACCAGATGCT CTGGTAAAGA 360
AAGCCATGGA TAAATATGAA TTATTTTCAG CTGAATGACC TTCAATTATC TCCTTTAACG 420
TTTAGACCTG GTTCTCTGCC ATAATCTTTC TTTGAGTACT TAGAGAAGAG ACCAACATAG 480
GGGCACCATT ATAGAGTGAT TTATGGAGGA CATGGACAAG GGTCATCTAT GGAATGTGAG 540
AGAAAACAGG AGGGGGAGGA GAAAAGAGGG AGAGGGTGCA TGCAAGAGAG ATTGAGAATA 600
AACTCAAGAT AAAAAATAAA AACATGGGAA ATATAGTTAT GTGGGTAGAG TCCTGGCTAG 660
GAGCCAGGAA TCCTGGGTGC CAGTCCTTCT TTTGGTATTA ACTCATTGCA ACAGGCTGAA 720
CCAATTCAAA ATACATTTAG TGTGAATCCA GTCTCTTAGC TTCATTATGC CAAGATTCTC 780
CCGCCATCAA ACAATGGGGC TAGTTTTTGT AGATTTTCTA ATTTCCAGGA ATCCTATATG 840
ATTTTATAGT AAGATGATCT GTGTTTCTTC ACCCCAGCTC TTTAATCCCA GTGTTGATAA 900
CTTTATCTCT ATGTCATCCT AAGCCCATAG TGAAATGTCT TGAAGATGCT GAGACTGAAT 960
AGTCATTTTT GTCTCCCCAT CCCTTTTCCT GGAAATTCTT CTTGACCACC TTTCCATTTA 1020
TTAAACCACT GTTTTTCAGC TTAATGACTT TATTTTGATA ACTACTGCAT GCCCTTAGGA 1080
AAAGTCAGCA GTGGTGGTGC CAGCAGGAAC TATTTATAGT AAGCAAACTG TTTATGAAAA 1140
ATGTAATCTT TAAGAGAAGA CTTGCTTGTA GACTTACTTC ATCTCTTTCA TTTCATTTTG 1200
CTAAATTTTT CTCAACAGTT TCAACACCCA CAAGAACATC TCTCTCTAGC 1250
|
| |
|
|
|
