| Tag | Content |
|---|
EnhancerAtlas ID | HS059-00486 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:16746620-16748000 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr1:16747394-16747412 | TGAAAGTGAAACCCATCA | + | 6.39 | | RREB1 | MA0073.1 | chr1:16747211-16747231 | GGGAGGGTGGTGGGTTTGGG | - | 6.21 | | RREB1 | MA0073.1 | chr1:16747212-16747232 | GGAGGGTGGTGGGTTTGGGG | - | 6.64 | | ZNF263 | MA0528.1 | chr1:16747931-16747952 | TCTTCCTCCTCCTGATCCCCC | - | 7.03 | | ZNF263 | MA0528.1 | chr1:16747928-16747949 | CCCTCTTCCTCCTCCTGATCC | - | 7.17 |
|
| | 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 |
| GH01I016420 | chr1 | 16746901 | 16748580 |
|
Enhancer Sequence | CAAGGTAGGG CTGTCATGGA GCCTGGAGAA GGCAGCATTG AGGAGAGAGG GAGCCACTGT 60
GTCTTCTGCT GTTGCGAGGT GGGCTCTGTA AGGACAGAGC TCTTCCATTT GATAAGCCAG 120
ATGGAGATTA TGGAGACCCC GATAAAAGCT CTCATATGGG GATGTGTTGA GAAAAGACAA 180
GCGGAGGAGG TGAGGGGGAC AATTATTGAG GGATGGGGCT GCAAAGGGGA GCAAGGAAAG 240
ACGGCTTTTG ACGCCAGGTA TGTTTGTACA CGCCTGTAGT CCCAGCTACT CAGGAGGCTG 300
AGACTAGCTT GAACCCGGGA GGTGGAGGTT GCAGTGAGCC GTGATCACAC CACTGCACTC 360
CAGCCTGGGC AACAGAGACT CTGTCTCAAA AAAAAGGAAA GAAAGAAAGA AAGGCAGCTT 420
TTGATATTGT GGAGGCTGAG CCATGTTTGT ATGCTGATGG AATCGTCCTG TAGTAACGCA 480
GAGAGGGATC ATGTGGTGGG GGGAGGGGAC GAGAGCTAAT GAATAAATGG GGAGACAGCC 540
ATGGGAGCAG GGGCCCATCT TCACAGCTCC CATTGCAGCC AAATCAAGGC AGGGAGGGTG 600
GTGGGTTTGG GGATGCTTCT TCTCATCTGA TGCTTCTGTT TGTCAGTGAC ACATGAGTGA 660
GATGAGGGGC GTGGGGGATG CTGTTGTGAA ATGATGACCT GGAGCGGAGG GAGGGCGGTG 720
TGGCCAAGGA AAAGTGAGAC TTGCAGGCAG CATCTGACAT GAGTGGTTAA TGCTTGAAAG 780
TGAAACCCAT CAATAAGACA GGATGTTCTC CAACCGCATT AAGCTGCTCA ACATGGGTAC 840
AAGGCTGAGT GAGTTTAGCC AGGGTGGGGT TTTGCCAATG AACAGAACAG GATGAGACAG 900
GGCAGATGCT GGCAGGGCAT GCATGCTAGT GACTGTGTAT TTGCAGGTTG CCTGGTCAGG 960
TCAAAGAACT AGGAAGTGGC AGAGCTTGGG GAGGGAAGGA TGGCTGGGAG GGGTCGGGGA 1020
AGCCTCCCAG GTGTTCAGGG ATGCTTTGGA TTGTGTGGCT GTGGCCGAGG GCAAATGGGT 1080
GGAAGAAATC CATGCTGATG TGGAACAAGC CACCACCTGG GATGAACCCA AGGGCTCCAG 1140
AGTGTAAGAG CATTCTTGAT GCCCACCCAG AATACACACA CATGCATACA CACAGGCACA 1200
GGCACACACA CACACGTGTG CACATCCATG TGCACTTTAA CACACAGCCA CACACACCTT 1260
CCTTGGTTTG ACTCCAAATA GGGGTTTGAC GTGCCACATC CGCTTCTGCC CTCTTCCTCC 1320
TCCTGATCCC CCCTGCCTTT CTCCTACACA GCTCGTCCCC GTTCCCCCTA TGGCCCTACT 1380
|
