| Tag | Content |
|---|
EnhancerAtlas ID | HS095-09061 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr14:59658280-59659620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr14:59658752-59658763 | AGAGGGTGTGG | - | 6.02 |
|
| | 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 |
| GH14I059192 | chr14 | 59658719 | 59659190 |
|
Enhancer Sequence | ATAAACCAAA ACTTGTCTGG CATAAAAGGC CTTCTATGTA TTTGAAATAG ACATATTTCC 60
TAATTATTTG CTTTTAGAAT ACATTCACTC ACATCGACTG TTTCTTTGTA GTTACAATTT 120
CTTATTACCC CTGAACCAGG CATTTCTAGA TTTCTCTCAG TTGCACTATC CTTGGCCCAG 180
ATAATCTTCC CAGGAGGTGT GTGACACGTG AATAGGGAGA GACACCAAGA GAAAGATACC 240
CAGAAGCCTT TGCCAGGCCA CCAGTGTCTC CCAGAAGAGC TGGGAGACAA TAGTCCTCTC 300
ACCTGAGGCA GAGCCGTTCC GTAAACAGGA TCAGTTGTTT CAGGCTGGTT GATGTGAAAG 360
AAATGTGAAA GAACATTTGC CCAATATTTG TAACATGTTA CCATCCAGTA GTCTGATTCT 420
GTGGGTTTTC AGGAGCATAA ATTAGTAAAT TAGTGAGGAG GTGTGATAAT GAAGAGGGTG 480
TGGTGGGTCA CATCCTTGGG TGGTGCTTAC AGGAGCTCCA TGAATAGGTG CTAAGGAATT 540
TGAATCCTGG CTTTCTTGTT TTGTGGACAT GTTCTGCTTG TTAAGGGGTG TGTGTGTGTG 600
TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGGTTTTGAG CTACTTTGTT TAAAAGGCTG 660
CTTTTAGTGT TGGCACTATG GTCCTTAAAA CAAATAAGGT GTTTACAAGC AAAAGTTCTG 720
ATTGAAAGTG TTTCATTTTG TAAATATTTG GGAGATGGCA TAAAGAGAAA CTTGAGGTCT 780
TGTGTGAAAA CACTTTAAAG TTGCAGCTGT TGGACCAGAG GAAACATGCT TTTCCAACAA 840
AGCTTGGTAT CCTTGAGTGC CCTAGGTGTT TGGTTCAGGA AATAATCACA GAGCTTGTAA 900
CTGCTGTGGG GCCCTCCCTG GCTTCAAGCC GTGCTCTGGT ATTTCCAGTG TTAAGTCTAT 960
CCTTATATTG CCGGAAACAA AGCAAGGTGT CCAACTTGGG TTAGCAAACT TGTTTTCTCT 1020
CTAGAGGGGA CACCAGTCAA AATAGAAGTT CTATATTCTG TTGTGATTTT TTCCTCTTTG 1080
GATGAGGAAT ATGGTGACTT ATTTTGGTAT TACAATTTCT AACTTGGTAA TAGAGGTAAT 1140
ATTCTAAGTG AATACCAATC TTAAGTACGC ACAGCATCTG TTGTAGTGGT TTCAAGACCT 1200
CAAAGTTTAG GCCGGGCGCG GTGGCTCAAG CCTGTAATCC CAGCACTTTG GGAGGCCAAG 1260
TCGGGAGGAT CATGAGGTCA GGACATCGAG ACCATCCTGG CTAACACGGG GAAACCCCGT 1320
CTCTACTAAA AATACAAAAA 1340
|
