| Tag | Content |
|---|
EnhancerAtlas ID | HS034-25751 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr6:16635880-16636850 |
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 | ACACAGTCGT TATCTGATTC TTTAGGCAGG ACATTGACCA GATAAATAAA TATGTCTGAA 60
TCTGCAGAGA AATAATTTCA AAAGGGCTTC AGAAGGAGAA GGAAAATCCA CTGTAGCCAG 120
AAGCATCCAA AAGCATCCTG AAAACATGAG TGGAGGAAGG CTGAGCAGGT GTGGGCTGGG 180
GAGGCAGGCA ACCCCGCACA GCAGCCAGCA CAAACACAAA GCGACGACGC CCACTGTGCT 240
GGGGAAGCAC AGGCAGCACA GTCCGTGCAA GGGAAACGCG GCTCCCTACA AGGTGTTTTC 300
AAGGTTCCGG TTTCCCCAGA GCACAACCCT AACCTCAGGC AGTGCACAGT TCTCCCAATA 360
AAAGTCACTC GCCCGTGGAG ATCACCGAAC ACCTGAATTG ACACCACGGG CACTTCCAAC 420
CTGTGTTCCT GACCACCCTC CCCATGACCT GCCTCCCTTA CATCATTTCT GTTTTCCTTT 480
CCCATGGTCC TGTGACTTCT CTTACTCTTT CAAATGCAAA ATGTCACAGC TGAAGGGAAG 540
GAACCTCCAA GGATGATCTG GGCTACTGCT TTCTTCTTCA TAGGGGAGGA AACTGAGATT 600
CCAGAGAGGT TGGTAACTTT CCCAAGGTTA CAAAATTAGC AGTGCAGCCG GAACTGAAAC 660
CTACATTGTG TGACCACTCT CCTCCTCCCA AAGCAATTTA GTTTCCAACT GGACCTCATC 720
TGCCTACTTG TTTCTCCCCC AGCCCCCAGG CAGCCCTTCA CTGTGGCTGC TGAGTCATCA 780
GGATGAGCTT TGTTCTCAAG CAAGCCACTG GGACAGGCCC TCATGTCTTG AGTAGGACAA 840
AGTATATTTG GCCACTCCCC ACTTTGTGGT CACCCTGCTC TGCCTGATGC ATGGGCACCT 900
TCTGCCCATG ACAACTGTCA TTCGCCCTGA ATAGTCTATG CCATCACACC TCCTTATGGC 960
TACTAACATA 970
|
