| Tag | Content |
|---|
EnhancerAtlas ID | HS034-25054 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr5:141657190-141658620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| DUX4 | MA0468.1 | chr5:141657267-141657278 | TGATTGAATTA | - | 6.14 | | IRF1 | MA0050.2 | chr5:141658233-141658254 | AAAGGGAAAAAGAAAGAAATA | - | 6.73 | | NEUROD2 | MA0668.1 | chr5:141658446-141658456 | GCCATATGGT | + | 6.02 | | Stat6 | MA0520.1 | chr5:141657742-141657757 | AGTTCTGAGGAAGAC | - | 6.38 |
|
| | 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 |
| GH05I142278 | chr5 | 141658317 | 141661861 |
|
Enhancer Sequence | CTCTGAGCCT CAGTTTCATC TGTAAGAGGG GTTTGACCAT AGGACCTACT CCTCATACAT 60
CCCTATCACT GATGAGATGA TTGAATTAGA TGACACAAGT GGAGTTCTAG TTCAGATTCT 120
GGCACAAAGC TGGTCTTTAG GGAATGGTAG TTATTGTAAC TAACTTTAGC TCAAGAGGTG 180
AGCTTCCTGA CAGGGGACTC CATTGCAACC TTTCTTGAAT CTATTCATCC TCCCTCTTTG 240
TTCTTCATTC ACAGCAGGAA GGGAAAAATT CCTGATGTGC AGTGGGAGAA ATTTAAGTTG 300
GATCCAGGCA GACATGTGCT GGTAAATGTT TAACAACCAG CTCTACAGGA AAATAAAAGC 360
ACTGATCCGC GGCATTTGCG GATTTCCACC CCTCCATGGC TGATTTCAAA CAACCAACAT 420
GATGTTGCTG AACAATGGAG TTGGGACAAG ATGTGTGCAG TTGGCTCTTA TGAGCCAGCA 480
CCAGTACACC ACTGGACTCA GGGGAGGATA CCTTTAAAAT ACTAGGGAGT GGGGAAAAAC 540
AGGTGGTTCC TAAGTTCTGA GGAAGACTGT CAAAAGAAAT TCCTCAAGTA CTGTTGAGAG 600
GATGGGGGAT GAACTCACAT TATGCTTTGA CTTAAAACTC CAGAGTTCTC TTTAAATGAT 660
AGCCTTTAAA TCCTCCCTCC TGCTCCCACA TACAGCCAGT CAGGTCTCTG GCTCTATTTC 720
TTCCTTAAAA TATCCCCTGC AGGCCGGGCA TAGTGGCTCA TGCCTGCAAT CCCAGCACTT 780
TGGGAGGCTG ATACGGGTGG ATCACTTGAG GTCAGGCAGA TCTTGAAAGA CCAGCCTGGC 840
CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAT TGGCTGGGCG TGGCAGCATG 900
TACCTGTAAT TCCAGCTACT GGGAGGCTGA GGCAGGAGAA TTGCTTGAAC CCTGGAGGAG 960
GAGGTTGCAG TGAGCCTAGA TCATGCCACT GCACTCCAGC CTGGGCAACA GAGTGACACT 1020
GTGTCTCAAA TAAAAAAAAA AAAAAAGGGA AAAAGAAAGA AATAAAATAT CCCCTGCATC 1080
CATCCATCTC TTTCACTTCA TGGCCCGCAT GGCCACCCCA GCCCATGGGC TCAGACTGTC 1140
AACTCTGAAA TACTGCTCCT TGTCCCTGCC CCTTCCCACC CATTCTGTAC TAGAATGGAC 1200
CAGCCATGCC ACCCCTAAGC CAGCATTCAT TGCATCATCC TCATTCCAGC TTCACTGCCA 1260
TATGGTTCCA GGCTTGCTGT CCCATTCATT GTAAGTGCTG CTGCCTGGCT GTCCCAGCTT 1320
TCACCTGGCC CCTCAGTCTG GAAGTGGTCT ATGTGTGAAT CTCAGATTTC CTGCTTACTA 1380
GTGATATGCT CTTGGGAAAA TTACAGAACA CTTTCTGAGC CTTCACTTCC 1430
|
