| Tag | Content |
|---|
EnhancerAtlas ID | HS042-18213 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr16:84390100-84391280 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr16:84391072-84391086 | CTGAGTCATTTTTT | - | 6.45 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23368 | chr16:84389204-84391410 | Colon_Crypt_1 | | SE_24110 | chr16:84389654-84390234 | Colon_Crypt_2 | | SE_24110 | chr16:84390765-84391279 | Colon_Crypt_2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 4 | ID | Chromosome | Start | End |
| GH16I084356 | chr16 | 84390221 | 84390310 | | GH16I084360 | chr16 | 84390501 | 84390530 | | GH16I084357 | chr16 | 84390890 | 84390990 | | GH16I084359 | chr16 | 84390991 | 84391238 |
|
Enhancer Sequence | TACAATTTCC CCTTCTGCAA AATGGTGAGC GCAAAATGCT GAGCGCAAGC AAATTGTTAC 60
AAGGATGAAG TGAGGGCAAA ATCTGAGCAC AGGGCCCGGG GGCAGGTCAG CGGTATCGCT 120
GGCTCACACT GGGCTATTCT TATCCTCCCA CAAGGTCCTC TGGCTCTCAT TAAATATTTG 180
TTGAATGAAT TAACCAGCTT TCCTACTGGT TTAACTGGGT TCATGGGACC CGCCCCTGTA 240
CCGCCCAAAC TGTTGATCAA AAGTCCCTTG GTGTCCAGGC TGGCTGGTAA AAATGACAGC 300
CAGACCCAAT GCAAAGAGCC AGCTGCGGCA TCCAGTCCCA TCACCATGGG AGCTCCCCAG 360
GCTTCCCGGG GTGGGCGCCT GAATGTAGTC ATTGTCCCTG GGTTTTGGCT CCCTTCAGGT 420
TCACTGGGGC CAAGGCACTC TGCCGCCTCG GGCCAGGGCT CTCTTGTTCA TTCAACACAG 480
TAAACATTCC ATTCAAGCCC CTACTATGTA CCAGACACAC TTCCAGGTGC TGGGAATAAA 540
GCAGGAAAGA TAACAGATCT CAGGGAGCTG GCAGTCCAGG GGGGGCACGG GCAAAAAGCA 600
AACAGACCAA GTCAGTGGTA GAAGGGCTTT GGGGGAAAAT AAAGCCGAGT AAGGAATGGA 660
GAGAGACAGA GGTGTGTTTA CCTTTGTATT TTCAAATAAT TACAGATTTC CAGGATGTGG 720
TCCAGGGTAC TCTTCACTTG GCTTCTTCCC ATGGTTACAT CTTACATAAC CACAGTGCCA 780
AATCTAAGCC AGGAAACGTG TGCAGCTACA ATGTGAGCAC AGCAGTCCCT TGGTATCCAC 840
GGCGATTGGT TCCAGGACCC TGTCTCCCAG GACAGCAAAA TCCCAGGGTG CTCAAGTCCC 900
CCAGTCAGCC CTCCCAGTAT CCGCAGGCTC CTCAGAAACC TCAGACGGAG GGAGGGCCAC 960
TGTGTGTGGT TTCTGAGTCA TTTTTTCACT GTATAGATTC ATGCAGCCAC CCGTACAGCT 1020
AGGGAAGAGA ACGATTCCAT CACGCCTAGG TCCGCCTTGC ACAACCTTTG TGGTGACATC 1080
CACACCACCC CTAACCCCAG CATCCACTCA TGTGTTCTCC TTGTCTATAA TCTTGTCATT 1140
TCAAGCATGG TATGAAGGAG AATCACACGG TATGTGACCT 1180
|
