| Tag | Content |
|---|
EnhancerAtlas ID | HS147-01853 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:66277630-66278800 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:66277643-66277655 | AAACAAACAAAC | - | 6.32 | | IRF1 | MA0050.2 | chr1:66277929-66277950 | CTTGGCTTTCAGTTTCTGCTC | + | 6.44 |
|
| | 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 |
| GH01I065811 | chr1 | 66277261 | 66278795 |
|
Enhancer Sequence | AAAAAGTAAA GCCAAACAAA CAAACCAAAA AAAACCCCAG GACCATTAAA AGACAAAATT 60
AACATATTGT AGTACTGAGG TTTCAGTGAG GAATTAAGCT TAGTTCCTTT CATTTCACTA 120
AAGAAGTTTT AACCCTTGTG GTGGCTCAAG GGCTAGGGCT TCTTTTGGCT TTGAGAGCAG 180
ATGAATTGAC TCATCCCTGA CCTCAGCCCT CAGCCTTCTG CTGATTTGGC ATCTCTAGCT 240
TCCTTCCCCG AGGTCTGACC TTTTGCCTCA TTTCCTCTGA CTCAATTTTG GGTTCTGTTC 300
TTGGCTTTCA GTTTCTGCTC TGAGAGTTCC TTTTCTAAAT TTCTGGGTCC TCTTGTAGGT 360
TAGTTACTCA CTTGTTTCAG TTTCTCTGCT GGTCTCCTTC TTAGGGTATG GCCCTCCATG 420
CTCTGCCACA CCTGGGTTGC ATCAGCTGCT CAAAGGCAGC ATTTCTCACC TGCTGCTGCT 480
CTCCCTGATC CAGGGCCAAC TTGGACAAAT CCCTTCCAAA TGTAATTGGC CATAATCATG 540
TAGGTTTTAA CTATAGGTTG GTGGCATTAA ATTTCCAAGA CAGTAAAATG TCAGGGTGGA 600
AATTCATTGT TTTTAGATAC TGGAGGGACT TTCTGTGTTT TAAATGCCTC TCAATTATTT 660
TTTTCATCCA TTGGCACACT TTGGAATGTT AATATTTGTA GTAAATACTG AACTACATAG 720
ATAATGCTGT TTGTGGTTCT AGGAATTACA TGCCTATCCT AGGGACTGAG GGGACGACTG 780
TCTCAGCCTC CTATATGATA TTATGTATAG AAATGCACTG GTTGAGAAGC TCTATTCTAA 840
AGTCTCCATG AAAACACAAA TAGATAGCAC TGGGCAGGGG TTGGGAGAGA GTATAACACC 900
TTAAACAATT ATTCTCTAGC TTCTTTATTT CTATTTGCCT GTCAACTGCT TTCTAAGGGT 960
CCTAGACAGC CCTGGAAAAG TTGCCCCAGG AATACAAAAC CTTAAGAATG AAGATAAGGA 1020
CACTAAAGTT TCTGTAGGGG CTGGAGAGGG AATACCTAAA TCTATTCTAA GACATGTTGG 1080
GAGATACTAA AACTGGAACG AGATTGGGAA CAGGCAGAGA GTTAGGAGGC TACCGAGGGA 1140
GTTCAGGAAT GAGGTATTGA GGGTTTGGTT 1170
|
