| Tag | Content |
|---|
EnhancerAtlas ID | HS133-11886 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr16:84172310-84173860 |
Target genes | | Number: 15 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TCF7L2 | MA0523.1 | chr16:84172927-84172941 | GAAGATCAAAGAGA | + | 6.48 |
|
| | 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 |
| GH16I084137 | chr16 | 84171353 | 84173977 |
|
Enhancer Sequence | AACCACAACT GTCCCCAAAC TAGGAAAAGA AGAGCAAGTC CCTATTATCT TTTAAGCATT 60
TTCTACTTCT ACAGGGCAGG AGTCATCAAA AACCTACAGG AAACGTTACA ACTACAAAAG 120
CGTCACGGGA CAATTATGGT CAAAACTGCA AGTAGCAAAG TCACCTCTTC AAAGCACCAC 180
TGCTGTGGCC TGTAACATGA TCCCACTCCA CAGTGAAGGG GACTCCACCT AGCAGTGTAA 240
AGGGCAATCA ACTCAAATAG AAAAACCTTC ATGTACCAAG AGTTCTGGGA GGAAAGTCTT 300
GGCTGAAACA TGGACATTAC CAAGCTATCC AAATGCGTGT GACGTGGGGC GGGTGGTGAA 360
AGAACACAAG GCAGACTGGC CAGGGTTTTA AAGAAGACAA AGCAAGCAGG ATGGAAAAAA 420
AGACAATCAA AGCATTAGCG AACGACAGTG TGGTGGGCAC AGTAATGGCC TCCAGGGATA 480
TCTACAGCCT AATCCCCAGA CCCTGTAAAT ACGTCACCTT ATGTGGCCAA AGGGACTCCG 540
TAGATGTGAC TGAGTTAAAG ACTCCGAGCT GGGGAGGGTG GGTCCAATGT CATCATGTGT 600
CCTTGTAAGG GGGGCAGGAA GATCAAAGAG AGAGAGCCAT GTGACTACAA AGGGAGAGGT 660
CAGAGAGAGC TCGAGTTGAG GGTGCTCTGT GCTGCTGGTT TCGATAATAG AGAGAGGGGT 720
GGGTCACCAG TGAAGGACGG GGGGTGGCCT CTAGAAGCTG GCAGAGGCAA GGAAAAGGAT 780
TCTCCCCTGG AGCCTCCAGA GGAACACAGC CCTGCTGACA CCTTGACTTT AGCGCAGTCA 840
CAATGACTTC AGATTCCCAT CTCCAGAAGG AAGAGACATC TGTGTCATTT TAAGCCACTA 900
CCTTTGTGGC AATTTGTTAC ATCAGCCACA GGGGATAAGG ATAAACAGTG GGAGGAAGGG 960
ATGGATGAAC AGTCAGTTCA GCTTTCAGGA CAGCGAAGAG ACAAGCTGAA AACTCTGCAA 1020
CCTCCCTTAA GCCAAAACCA CTATGTGTAT TCAGGAGCCA GAAAGTCTCA GAGGTTCCTG 1080
CCATCTTTGA CTGACCAGGG TAGACCTGAG GTCCTCCTCC TCACCAGCTG GGATTATCCA 1140
GCTTTTCAGT AAGGCTCCAG GGCGATGGCT GTTTTCATTG ATGAAAACAT TTTTCCAAAT 1200
AAATCTTAAT TTTTTCAGAG TGTGAATCTG TCTTGTGCTC AGTACTCCAA ATCCTCTGTT 1260
CTTCCTGACG TTTCAAGTCC CATGTCTTCT CCTCCGTTCA ATCACTTCCT AACAAGCACC 1320
AACAACATGT CAGCCCTGGG GAGAAACTTC CCTTCCTGTC CCTTCCCTTC CCAGGCCGTG 1380
GCACTGCCCC CACCTCTGAA TTCCTCTCCA CCTCTCTTAC CCATGTGGCA CTTAGCACAC 1440
ACTGCTTTGG ATTCTATTTA AACACTCAAC TTGCTTATAT CTTGGTTTCT TGGTTGTCCA 1500
AGGAGAGCAC AGGCCTCTGG AGGGCAGGAG ATGTATAGAA AACGAATTTT 1550
|
