| Tag | Content |
|---|
EnhancerAtlas ID | HS176-10657 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:120975940-120977640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nfe2l2 | MA0150.2 | chr12:120977293-120977308 | CAGCATGAATCAGCA | + | 6.4 | | RARA(var.2) | MA0730.1 | chr12:120976558-120976575 | AGGTTAAGGGAAGGTCA | + | 6.08 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 120976970 | 120977501 | | chr12 | 120976448 | 120976663 |
|
Enhancer Sequence | ACAGAGTACT GAGTTGAGGG GAAAACAAGC GTAAGGTGAA AAGATAGTTT ATCTTTTGTC 60
AAGGTGAAAA GAGCAAGAGT TTTCAGTATT CAAATATTTA AGTCACTTTT TTTCTCCCCC 120
TTTTCTACCT CGTGGAAGAA AGCCCTTTGG TTTCTATTCT GTAAACTGTC ATTAATGGCC 180
ATTTGCTTCC TAGCTACATG ATTAATTTCT TTGAGATTTT GTTCCAGTGG CTGGCTTAAA 240
TTTGCCCTTC ATTTGTACAC AGGAAATATG TAAATTTGGC TACCAGGATT TTCTTGATCT 300
TTCCGGCTAG AGTCGCATAC CACAGTTTCT TTGCCTGGGC TAATTGCCTG AACATTTATA 360
TAACATTCCT TTTCTTGATT ATATTCCTAC AGCTTCATTC CAGTAGTGTT AATAGGTATT 420
TCTGAGAACA TGCAGCAGTA AATATCCTGT GAATATAGCT CAGAGGAGAG AAGGTGGGTT 480
AGAAAGTGGG GAAAGTCATT TAGAGGGAGC AAAGAAAGAG AGGCAAGAGA GAAGGTAGGC 540
CGTTTATGGG CAGGCAGTGG ACTCTGGCCA GGAACCAGGC TCTTGTCCCA TCCCCCTGGG 600
CCGATAGAAC TGCCAGGGAG GTTAAGGGAA GGTCAGGTAT TATGAGGCAG TTATTTTGAG 660
GTTGGTGGTA TGAAGCACTG CCCTGGCATT CTTCCTGTTA TTCTGGTACC AGAAACCAGG 720
TTACTAGTGG TAATCTGCCT TGAAGAATGC CTCTGAGCTG TAAATGGACC TGGAGATTTT 780
AATGGCTTTG AAAATTGAGG TGATTTGAAG CCTTCAGTAA AACCACTTAG AGAAATTAAA 840
AGAATTTCAG GGCCCGTTGG CTGGATTCCT TGGTTTATAT GGCTTCATTG GAAGTCTAGT 900
GGGTGCTCTT GACAGGAACG CTTTGGATTT ATTAATGATA GGCTTTCAAA TCATAGTAAA 960
ACTGTGTGTC AGCCACTATG GTAGGCATTT TACAGAAGTT TTCTTTCTTA ATCCTCATGA 1020
TTCTATGAGG AAGTATGGTA GAATATTAGT CCTGTTTCAC AGAAAAGAAA ATAGAGGCTT 1080
AGCAGTGTTA AGAGTGATTT GTCCAAGTAA ATTTTTATGA AGTCCTAGGC GGTATTTTTC 1140
AATAAGCTTT GTATAATCAC ACTTAGCAAG CAGATAACTT ACTGGCATGT GCATCATTCC 1200
TGATACCACC TCTCTCTTCC TTTCATTCAG AATTACTAAT TTCAGCTGGA TTCAATTTGT 1260
TGTCAGTTGA TTCTGTAGTA AGGCCATATG TTGCCCCTCT GGAGGTGCTT GTCAACTACT 1320
CTGGATGATG GGTAAGCAAC TTGCTTGTGA TTACAGCATG AATCAGCAGC AGAAACTTGC 1380
TGACTGGTAT TCTGACCTCT AGGCCGAGCC ACCTGTTAGA ACTAGAGCTA GAAATGAAGA 1440
TGCCAAGTAA TTTAACTGTG AAAAACTTGT GGCCCTTAAT TTGGTAATGG GGGGAGGCTG 1500
AGATATACCT ACTGCTACTT GGTGGAGACC TTTCCATTAG GGAAATGTGG AACAACTGAG 1560
AAGCTGGGTT AAGTTTTTAA GTCATTTATT TGTCGACTCT GGAGCCTGAG TTTAGTGGTC 1620
TTGTCCATTT TGGAATGTGT CTTGACAGTA GTTCTTGGCA GTTGTTCTCA GTGGTGGCTG 1680
TGCATCAGAA TCTCCTCAGG 1700
|
