| Tag | Content |
|---|
EnhancerAtlas ID | HS047-08175 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:67217090-67218490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr12:67218161-67218175 | ATGAGTCATTCCTT | - | 7.34 | | NFE2L1 | MA0089.2 | chr12:67218157-67218172 | TATGATGAGTCATTC | - | 6.17 |
|
| | 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 |
| GH12I066823 | chr12 | 67217074 | 67218790 |
|
Enhancer Sequence | TGGTACATGT TGGTAATGGT TCTCAAGTTG CTGCCTTTGT ATTTGTTTTG GGAGATTAAA 60
ATTCCTTGAG GATAGAGATC TCTAGATTTC TATTTGGTTG ATTACCCAAT AATGTCTAGC 120
AAAGTACTTT GCACATTAAC ATTTTCATGA TAAAAATGAT CAATGATCAT TTACAGCTTC 180
CTTGGTTTAT TAAAACAATT AAGATTCATC TTTCTCCTTC ATCAGTATTT AGTACATACT 240
CTGGCACCTA ATACACCATA TCTATCTCTA TAGCAGAAAA ATTAAGATTT TGTACTTTGA 300
TAAAAAAAAT CAGAGACATT TAATAGAAGC AATATTGGAA ATCAAGAATT TACTCAGTAA 360
ACACCAACCA TAATACCAGG AAATCATTTC TCTATACAAA TGATTTCCCA GGCCTGAGAA 420
TCCTAGCACT TACACCACTC ACAGAATTCA AGGAAAGAAA GAGTTCTGAT TTGGGGTGAC 480
AGCATCATCC TCTTTGCCTT TCTCTCCCAC AATATAATCC CAACAGATAA CCACACGCTT 540
TTTACTGTCA TGTTTGGGCT AAAATTCTTA TCAATTGAAC AAGATGTAAA ACAGAAAATC 600
CAATGCCATC CTCAAACTCT GAAACAGACA GCCTGATGAT TCTGAAGTGT AACCAGTTCT 660
AACTCTATTA ATAGCTCTAT CCTTTCCAGG AGAGTACACA GAAACAGGCT GCAGCTGCCA 720
CAAGGCCCTA ATGTTTCATT CTTTGTACAA GTCTGACAAG TTTTCAAGTT TAATAGCATT 780
AGCAATGATG TGATGTAACC GTGGCAGAGG TAGCCTGAGT CTGCCAGGAT TTTTGAAAAG 840
GTGGGTGGGG CACAATCCCT AAACACCTAA TGGTTTGGGA TAAGGCATTT TAATCATTTA 900
ACCAAAAAAA TCAGACATAC TAACAACCCT CCCCATCAAG GTGGAGTGCA AAGAAGCAGT 960
AGTTACTGGT TGAAAGGTGG ACGGTTTCAG ATATATGTGA ATAAAGACAT AGCCTGTGCT 1020
GTTGAAGCTC CAGGCCCAGG TCATGCGTCT ACACTAGGAC TGCCTCATAT GATGAGTCAT 1080
TCCTTGCATG GCACTGGATA ATTACTCCAT GCCTGAAGCA TTTTACTGGG TCTTTTTGAT 1140
GTGACATAGC TCAGAGGATT TTACAGGGCT TTGGCAACGC AAATGGCCTA CTCATCATGA 1200
AGCCCAAACA CCACCTCCCT CCCCACCAAG CCGAATGCCC TTTGCATAAC CTGGACAAGT 1260
GGTTGTCCAT TTCTCCTTCA ATGTGTCTAT TGATGAGAAG GTCACACATT TAAATAACTG 1320
TGGTTTATAT AGAGGAAGCA CAGGGAAACT CATGATTCAA GGATAATTAT AACCAAGAAA 1380
AGGCCACTCG AAGTGAATTC 1400
|
