| Tag | Content |
|---|
EnhancerAtlas ID | HS047-15853 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr18:29628670-29630120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr18:29629565-29629586 | CGGGGAGGAGGAGGATGGGGA | + | 6.49 | | ZNF263 | MA0528.1 | chr18:29629571-29629592 | GGAGGAGGATGGGGAAGTGAA | + | 7.36 | | ZNF263 | MA0528.1 | chr18:29629568-29629589 | GGAGGAGGAGGATGGGGAAGT | + | 7.69 |
|
| | 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 |
| GH18I032047 | chr18 | 29627919 | 29631200 |
|
Enhancer Sequence | GCCTAGGGAG TTGGCAATTG GAATGGCTAA GTAGGAGCTT GTTAGGTGTT GAGGGAGCAG 60
AGCCGATGGT CACGGGCTTT TCCTGCTCAA GTTGCTCTGT AGGAGGAACT GGGCTAGGGA 120
GTTGTTTCAC AATAGGTCCC TGGGGAGCTA GAGGAAGTTA GAAGAAAGCA TAAGGATGGA 180
ATGATAGTGA CTACTATCAC TGAGTTTACT GAGTTATAAG TATTTTCTTG TCTCCTAGCA 240
ACTCTGTGAA GAAGGTTGAA CCCTGACCAT TAGTACCCAG GGTGCTGCTT TGGCTGGAAG 300
AATGCCAGGC CCTCTGGACT GTGGTCCTAG GCTGCATCTA AGCAGCAATC TGGGGCAGGC 360
CGTGTACTGG TCAGTTCCGT GGTACTGTGT ACCTGCTCCA GCAGAAATCC AGTCCACATG 420
CTGCTCAGTT TGGCCCAAAT TGAAGGTGGC CCATGAAGCT AGGTCCTCCA TGATTTTACA 480
GGTCTTCAGG GTCATTGAAG ACAGCTGACC TAAGCAGGGA AACAAACTAG GAATGGTGGA 540
ATCAGATTGC CTGTGGGATT TTGTAGTTAA ATCCTAGGCT TTAAAGGGGA TAGGCTTGGT 600
TCTAATCCCA GGAAGTCTAT TAAATTCTGT CACTGTTTCA TCATTTGTAA AATGGGGATG 660
GTGATGACAT TCATGCCTTT TTCACAAGTA GTAAATGAAT CAGGCATATA ATAAAGTAAG 720
CACTCTGTCT CCTGGTGATC ACTCCATTAA TAGAAGAGGG TGGTGGTGAT AGTGGAGGTT 780
CACTACACTT TTTCAATTCT ATAAAATCAG GCCTAGAGAA GATTTCTTAG AGGAAGTGAT 840
GTCCTCTCAC AGTTAGAGAA CCCACATGGG GTGGTGGTGT GAGTCGGGGG GGTGGCGGGG 900
AGGAGGAGGA TGGGGAAGTG AAGTGGTAAA ATCTCACCAC AAAGACCAGG ATGCTATCAT 960
GGCCTTGAAG CAGGAGCAGA TTGTTCAGAA ATCCAAGGTT CTGTAATACC CTAGGGCTGT 1020
CTAGAGGTGG TAATTGGAAC ACAAGACCTT CAGGTGTCCT GTGTTAGTGT TTCACTCTTG 1080
AGCAGAAGCT CAGGAGCATG TCACTCTGAA GGATCTAGAG CCACTAGAAG TCATGATTTA 1140
CCCCATGGTT AGGAAAAGGC AGGGGACAGA TATGTGGTAT AGCTGGGGTT CACGTGCTTA 1200
GGGGTCCCTA ATGGGGACAT GTGGGTGAAA ACACACTGAG GGAAGTCCTG GGCAAGGAGG 1260
GCTGGGTCCA ATGCTGATTC TGGATGGGTG TGGAAGTTAA CCAGGAATTA TTGCTTTAAA 1320
GGACTGGATT ACAGGTTTTG CAAGCAGATA AGATCAGTGA CATCATCTGA CTTACCTCAC 1380
ATAAGAGGTT TCCTGGCATT TAGAGATTTC CTGGGTAAAT GATTCTTCTG ACTTCCAAAA 1440
ATAATTAGAT 1450
|
