| Tag | Content |
|---|
EnhancerAtlas ID | HS044-07924 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr2:242318370-242319870 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:242318903-242318924 | CTTTTCTTTCTTTTTTTCTTT | + | 6.5 | | ZBTB18 | MA0698.1 | chr2:242319079-242319092 | TAGCCAGATGTTT | + | 6.13 |
|
| | 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 |
| GH02I241378 | chr2 | 242318015 | 242319955 |
|
Enhancer Sequence | TAAAGAATCT TGTTTTTGAG CCATAATTGT TTTAAAACCA TCTGAAAGTT GTGTGTCAGC 60
TTGCCTTGTC TTGTGTGCTA AGTCATCGGG TAGAAATACT TTCAGCTCCA AACCATGCCA 120
GGTGTGAAAA GTGTCTAACT CCATTGCTGG ATGCAGTGGA AGGAGAGTTG AGGTGCATAA 180
CTGAGACCCC GTTCTAGAAA GTCTTCCCAG ATCTTTAGAG GGTAAGATGT CTAGAACAAT 240
TATACTCTCA TTAATTCATA ATTAACTCTT AGGTTTAGGA GTTAATGCGA TTTAAAGGTT 300
TTCTATTATC TGAAAGTTAG TATTATGGAG AAGAGATATG TAATGATTAA AAGAACAACC 360
TGGGATGCAG TTTAAGGGTG TGAGGCCTTG CCCCTGGCAG CGAATGTCCT TTGCCTTTGC 420
TGACAAGTGG GGATTGCATC TAATGAGCAT GAGGGTTTTC TTCATTATTG TTCATCTACT 480
TTCTCACGTT CCCCTTTTCT TTAACATACT CACAGTTGTT AGGGTGGACT TTCCTTTTCT 540
TTCTTTTTTT CTTTAGAATT GCAGAGGCTT TAGGTTAAAT AGTGACAAGT AGGAAGACAA 600
ATTCTCAGTC ACGAAGTTCT GTGCTAGAAG ACTTTAACTT GCTATTCCAG TAAAAACTTA 660
ATGTTTTCAT TCTGGCAGGA AGAAATAGTC AAAATTCCAG AAAGTATTGT AGCCAGATGT 720
TTGTCATTGC TCCCACACGA ACATCCTAAA TATAGCAAAT AAACTGCCTT AGAACTTATT 780
TTGGTCTGAC CTCAGAAGAA AAAGTAACTC AGCTTCTGAA ATTTGGGGAT AATAGAGGTT 840
TTATACAAAA GCTCTTATGT GTTTCTGGGA TACCAAGCTA TTATGTGACT CTGCCCTAGC 900
TTTTAAAACC TGTTATTTTG TCTTGGAAAG TTGATCTATT CCTTTGACCC TGATGCTCAA 960
GAATGTGGTA GGGTGGTGCA CAGCAGAGAT GTGGACATTT TTATTCTTAG TTTTCCAGTG 1020
GTGATGTTGG CACTCCCAGA GCCAGCTCCC CCACCAAGCC CTAACACACA TACACAAGCA 1080
AGGTTGGTAA GTCACAGTCT GTGTTAGATT ACACAGCAAG GGCGACTGAT GAAGAAGTTA 1140
GGCCAGCAAA TGGAAAAGAA TAGGGAAATG TCATCCTATT GATCCCTGTA CCAGTGAAGA 1200
CGCCATGACA GTGGTTGTAT AGCAGAGAAT AACCAAGTTA TTTCAGGATC GCAGCAGAGG 1260
GTTGTGGGAA TGAAACTTGC TGACTGGGTC ACCTGGACTC GCACACCATT TGTTGAGCAC 1320
CTGAGAGTTC TAGCACCCAA TGTTGATCAC ATATCAGGTG ACACAGGCAG TGGCTGACCC 1380
ATGTGAGCTG TGAGCGCCAA CTCAGAAACC CCTTGATCTA CTCGTGCCCA TGTAACTCCC 1440
CCATTTTTGA TCAGGAGAGA ATTTGATTCT GTTGTTATTT GATTCGTGGG AGGCTAGAAA 1500
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