| Tag | Content |
|---|
EnhancerAtlas ID | HS108-17807 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr17:74213220-74214880 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr17:74214017-74214032 | AATTAATGTTTAACA | + | 6.15 | | HNF1B | MA0153.2 | chr17:74214018-74214031 | ATTAATGTTTAAC | - | 6.04 | | NEUROG2 | MA0669.1 | chr17:74213847-74213857 | AACATATGTC | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 74213477 | 74213975 | | chr17 | 74214196 | 74214299 |
|
Enhancer Sequence | AAAAAGAGCT CCCCAAACCT TCATCTATTT TTTGTTTGTT TTTGTTTTTC TGTAGAGATG 60
GAGTTTCACC ATGTTGGCCA GGCTGGTCTC AAACTCCTGG GTCAAGAGAC CTGCCCGCCT 120
CAGCCTCCCA AAGTGTTGGG ATTACAGGTG TGAGCCACCG AGCCCAGCCA TCCTCATCTG 180
TTAAAAGGAA AAATAAATTT ACTTATTGGT ATTTCATTTT ACAACCAAAA ATTTGCTTTT 240
TCCTTTCTTT GAAATGAACC CCTCTAGCAG CTTGCTTTCA TTTAGACAAA TGAGAAAAGC 300
AAATCAGCCT TTTTCAGACT GAATAAAGCT TTCTACTTGC TCAGTCTTTC TAGAGGGACA 360
AATTGGTGCA CAGCTATGTA TAGCTACTAG ATCATCAGAT ACCAACACCA AACACATCAA 420
CAGTCCCCAA ACAAGATGAC TTTTAGACAG CTTATGCATA TTTTTACTTC TTAACACAAT 480
GAACTGTGCT TCAAAATCAG TGGTGGGGGA AAAGAACTCT ACTAAAGTAC TTCTTTGCCT 540
ATTTGTTACC AGGAGAAACA CGTCACTCAC AGATAAACTG CAGAACTCAA CTAAAATACA 600
CCCTTGCCTA TTTGCTAACG GGAAAAAAAC ATATGTCACT AGTAGATAAA CTTCGAGTGT 660
TTCATTATTA GTGAGCTATA ATTTATTAAT CAAAACTCAT ATTCAGAATT CTTTGCAGGC 720
TTTAAAAAGT CACATCATAC ACATATCTCC AAGATTATAC GTAAACCGTA AGGTATGAGT 780
GGGAAGGAGA AAGGGGAAAT TAATGTTTAA CAAGTACATA GTTTTAGTTT TATAAAATAA 840
AAAAGTTCTA GACATCTGTT GCAAAACAGA GTGAATATAT GTAACACTAA TGAATGCTTA 900
AAAATGGTTA CTATGATTAA ATTTAACGTT ATGTGTTTTT TTGCCACAAT AATAAACACA 960
TAAATATCAA GAAAAAAAAC CAAAAGGTAT GAGCCAGAAT GATCAACACT AAGACAAGTT 1020
CAGTAAAATG ACTGACCTTT AAAGAAAGAA AGGCACCCAG GCAAAAAGTC AAAATTCTAG 1080
AGGGGAAGAA AATCGGTGTC ATCAGACTTT TCAACAGAAA CACTTTATGT CAGAAGACAA 1140
GGGAGTAACA TTCTAAGGTA GTCAAAGAAA GAAAAGCCCC TGAGCTCATC TGAGGAGTCT 1200
ACTAAGGAAT AAGCTTCCAG GCCAAGCCCA GTGGCTCACG CCTGCAATCC CAGTACTTTG 1260
GGAGGCCAAG GCAGGAGGAT TGCTTGAGCC CAGAAGTTCA AGATCAGCCT GGGCAACATA 1320
GCAAGACCTC ATCTCTACAA TAAAAAAATT AAAAAGTTAG CCAGGCATGG TGGCATGTGC 1380
TTGTGGTCCT AGATACTCGG GAAGCTAAGG TGGGAGGATT GCTGGAGGTC AAGGCAGGAG 1440
TGAGCTATGA TCACACCCCT GGACTCCAGC CTGGGCAACA GAGTGAGACT CTGTCTCAAT 1500
AAAGGAAAAA CAGGCCAGGC ATGGTGGCTC ACACCTGTAA TCCCAGCACT TTGGGAGGCC 1560
AAGGTGGGCA GATCAACTGA GGTCAGGAGT TTGAGACCAG CCTGTCCACC ATAGTGAAAC 1620
TTCGTCTCTA CTAAAAATAC AAAAATTAGC CGGGAGTGAT 1660
|
