| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03470 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:221273150-221274730 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf1 | MA0493.1 | chr1:221273767-221273778 | TGGGTGTGGCT | - | 6.14 |
|
| | 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 |
| GH01I221097 | chr1 | 221270473 | 221275210 |
|
Enhancer Sequence | TGAGAGAGGA AGGAGGCTAG GTTAACCATA AAACCCTCGG CTTTGATGGC TGAGCGAATG 60
GCACTGCTTC CAACTCACCT GGGGTTTGAC AGGATGGGTT TGAGGGGCCT CTGTGCCATC 120
TCTTCTACAG AGGACTGGAT GGGAGTCTAC TTCCTTCCAC TCACCAGTGG TTTGAATTGT 180
CAGAGGACTG ATGGCCTCAG CTCTGGTCCT GGCTCCTTCC TTTCCGGGTA ATCCCGCCAC 240
CACAGGTGGG CGTTTCACTT ATTACTCCTT TCTCACCTGC CTGTGGTGAA AGCGATGCCT 300
GCCCTAGAGG ATGCTGGGAG GAGTAATGCA GAGGTGGCTG TGAAAGGCCA CACAATACTC 360
GGGTCCTGAT GAGCAGCATC ACTTCTGTGA TGGCTGTCAT TTTCTCTGTT CAGCCGTTTT 420
CAAGAGTGTT AAGAAATAGC GGGGCTCTGT CCCAAGATTC CCCTTTCTTT GTAAAGCCTA 480
AGAAAGCAGA TGCTCCGGAT AAGCAGAGAA AACTCAGCAT TTCTGAGGGT TTGTGGGTTT 540
GAGTCAACAT TATGCTATCA CCTTTTAGTG CACTTAATAA TTAAGCTTAC AGTAGGTAGC 600
AGACAATGGC ATCGAGCTGG GTGTGGCTTC AGAGCCAGCC GAGTCCTTTC TTGAAGCTCT 660
ACAAAAGCCT CTATGATATT TCTCCCCACC TTGGAAATTT TTAAATAGTT TAAACATTTA 720
AGCAGATTTT AATGTTTTTT ATTTAAAAAA TGGAAGGAAT AAAAAGGCCA CAGTAGAATC 780
TTCAGGAAAG ACAGTGGTTG CAGTTCTGTA CATGTGAAAG TCAAAAAGTG GCTAAGAAAA 840
AGATGCTCCG CCTGCCACTA CTAAAAAGAA AAAACGTTTG CCATAAGCCA CCATGACTCA 900
GAGTTCACAG ATGGGAAGAA ACAGATAAAT TAGAGCAAAG TTCCTGAAAA TGTTCTGTGA 960
CTGATACTGC TTCCTGTAAG TGACTGGAAA GAGCTAGTGC TGATTTGAGT AGACATTGGT 1020
TCTTCTAGAA GAGCCAGAAG GTTTCACATG GATTTTTTTA ATGTTGGAAA AACCAGGCAG 1080
GAGAACAAAA AAAGGAGAAA AATTCTTTCC CCCCTTCTTT TAATATCGTT TTCAGTAGCA 1140
CAATGCATTT AAAGTAAGGC ACAGTTTCCT CAGAGTAATA TGGCCTCAGG ACATGATTTA 1200
GATGGAAAAT TTAAGTAAGA TTAATGCAAT TTATTATCCA ACAGGATATC CCTACAAGCC 1260
ACACTATTTG GCTGAATTTT AGATTCCCAA TCTAATATTT CAGATGAGAT TTCCAGATGG 1320
GTGTCTTATT CCTCTATTAG TTTAGTCAGG GTGATATAGA GTTTGTAAAA CAGGAGAGGT 1380
TAAACTAGTT TTAACACTTG ATTAATCATT GAAATTACTT TGTTACTGTT TGAATTCACT 1440
GACTTTTGTT TATTAAGTAA CTCCCTAAGA CCCAAAGCCA ACACAAACTA GAGGCACCTT 1500
TCCAGCTTTG CTAATTTATT TGATGACTTC TTCAAAGGAA ATTTTTTAAA AAGTAGTAAA 1560
TTTATGGTTA CATTGAAAGG 1580
|
