| Tag | Content |
|---|
EnhancerAtlas ID | HS002-08215 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr6:16635960-16636840 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MAFF | MA0495.3 | chr6:16636646-16636661 | CTGCTGAGTCATCAG | + | 6.16 | | MAFF | MA0495.3 | chr6:16636646-16636661 | CTGCTGAGTCATCAG | - | 6.1 | | NFE2L1 | MA0089.2 | chr6:16636645-16636660 | GCTGCTGAGTCATCA | - | 6.42 | | Nfe2l2 | MA0150.2 | chr6:16636647-16636662 | TGCTGAGTCATCAGG | - | 6.36 |
|
| | 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 |
| GH06I016635 | chr6 | 16635702 | 16637201 |
|
Enhancer Sequence | AAAGGGCTTC AGAAGGAGAA GGAAAATCCA CTGTAGCCAG AAGCATCCAA AAGCATCCTG 60
AAAACATGAG TGGAGGAAGG CTGAGCAGGT GTGGGCTGGG GAGGCAGGCA ACCCCGCACA 120
GCAGCCAGCA CAAACACAAA GCGACGACGC CCACTGTGCT GGGGAAGCAC AGGCAGCACA 180
GTCCGTGCAA GGGAAACGCG GCTCCCTACA AGGTGTTTTC AAGGTTCCGG TTTCCCCAGA 240
GCACAACCCT AACCTCAGGC AGTGCACAGT TCTCCCAATA AAAGTCACTC GCCCGTGGAG 300
ATCACCGAAC ACCTGAATTG ACACCACGGG CACTTCCAAC CTGTGTTCCT GACCACCCTC 360
CCCATGACCT GCCTCCCTTA CATCATTTCT GTTTTCCTTT CCCATGGTCC TGTGACTTCT 420
CTTACTCTTT CAAATGCAAA ATGTCACAGC TGAAGGGAAG GAACCTCCAA GGATGATCTG 480
GGCTACTGCT TTCTTCTTCA TAGGGGAGGA AACTGAGATT CCAGAGAGGT TGGTAACTTT 540
CCCAAGGTTA CAAAATTAGC AGTGCAGCCG GAACTGAAAC CTACATTGTG TGACCACTCT 600
CCTCCTCCCA AAGCAATTTA GTTTCCAACT GGACCTCATC TGCCTACTTG TTTCTCCCCC 660
AGCCCCCAGG CAGCCCTTCA CTGTGGCTGC TGAGTCATCA GGATGAGCTT TGTTCTCAAG 720
CAAGCCACTG GGACAGGCCC TCATGTCTTG AGTAGGACAA AGTATATTTG GCCACTCCCC 780
ACTTTGTGGT CACCCTGCTC TGCCTGATGC ATGGGCACCT TCTGCCCATG ACAACTGTCA 840
TTCGCCCTGA ATAGTCTATG CCATCACACC TCCTTATGGC 880
|
