| Tag | Content |
|---|
EnhancerAtlas ID | HS060-29192 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr6:16635970-16636840 |
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 | AGAAGGAGAA GGAAAATCCA CTGTAGCCAG AAGCATCCAA AAGCATCCTG AAAACATGAG 60
TGGAGGAAGG CTGAGCAGGT GTGGGCTGGG GAGGCAGGCA ACCCCGCACA GCAGCCAGCA 120
CAAACACAAA GCGACGACGC CCACTGTGCT GGGGAAGCAC AGGCAGCACA GTCCGTGCAA 180
GGGAAACGCG GCTCCCTACA AGGTGTTTTC AAGGTTCCGG TTTCCCCAGA GCACAACCCT 240
AACCTCAGGC AGTGCACAGT TCTCCCAATA AAAGTCACTC GCCCGTGGAG ATCACCGAAC 300
ACCTGAATTG ACACCACGGG CACTTCCAAC CTGTGTTCCT GACCACCCTC CCCATGACCT 360
GCCTCCCTTA CATCATTTCT GTTTTCCTTT CCCATGGTCC TGTGACTTCT CTTACTCTTT 420
CAAATGCAAA ATGTCACAGC TGAAGGGAAG GAACCTCCAA GGATGATCTG GGCTACTGCT 480
TTCTTCTTCA TAGGGGAGGA AACTGAGATT CCAGAGAGGT TGGTAACTTT CCCAAGGTTA 540
CAAAATTAGC AGTGCAGCCG GAACTGAAAC CTACATTGTG TGACCACTCT CCTCCTCCCA 600
AAGCAATTTA GTTTCCAACT GGACCTCATC TGCCTACTTG TTTCTCCCCC AGCCCCCAGG 660
CAGCCCTTCA CTGTGGCTGC TGAGTCATCA GGATGAGCTT TGTTCTCAAG CAAGCCACTG 720
GGACAGGCCC TCATGTCTTG AGTAGGACAA AGTATATTTG GCCACTCCCC ACTTTGTGGT 780
CACCCTGCTC TGCCTGATGC ATGGGCACCT TCTGCCCATG ACAACTGTCA TTCGCCCTGA 840
ATAGTCTATG CCATCACACC TCCTTATGGC 870
|
