| Tag | Content |
|---|
EnhancerAtlas ID | HS129-19355 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:37157230-37159340 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Atoh1 | MA0461.2 | chr2:37158779-37158789 | AACATATGTT | + | 6.02 | | Atoh1 | MA0461.2 | chr2:37158779-37158789 | AACATATGTT | - | 6.02 | | FOXC1 | MA0032.2 | chr2:37158822-37158833 | ATATTTACTTA | - | 6.14 | | IRF1 | MA0050.2 | chr2:37159296-37159317 | AGCTAGTTTTACTTTTTTTTT | + | 6.45 | | IRF1 | MA0050.2 | chr2:37158179-37158200 | AAAAAGAAAAAGAAAGAAGCA | - | 6.45 | | SOX10 | MA0442.2 | chr2:37157823-37157834 | AAAACAAAGCA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 37157607 | 37158871 | | chr2 | 37158014 | 37158618 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I036930 | chr2 | 37157624 | 37159042 |
|
Enhancer Sequence | AGTTTTCTCT GGCACATAAT CACTGCCTGT AGCCCTCTCT CTTAAAGACA GTGTCATTAT 60
CAGGCTAGGC GCGGTGGTTC ATGCCTGTAA TCCCAGCACT TTGGGAGACC GAGGCAGGTG 120
GATCACCTGA GGTCAGGAGT TCGAGACCAG CCTGACCAGT ATGATGAAAC CCCATCTCTA 180
CTAAAAATAC AAAAATTAGC CAGGCATGGT GGCGTGTGCC TGTAGTCCCA GCTACTCAGG 240
AGGCTGAGAC AGGAAAATTG CTTGAACCTG GGAGGTGGAA GTTGCAGTGA GCCAAGATCA 300
TGCCACTGCA CTCCAGAATG GGCAACAGAG CGAGACTCCA TCTCAAAAAA AAAAAAAAAG 360
TGTCATTATC ATTTGGTGAC ATCAAACTTT ACCATCAGAA TCACCCAGAT GACTTGTTAA 420
AACACAATTT TTTAGGTTCT ACCCTCAGAG TTGCTCATTC AGTAGGTCTG GAGTGGGGCC 480
CAAGAATTTG CATTTCTAGT AAGTACCCAG GTGATAATGC TGCTGATCTG GGACCAACCT 540
TGGAGAACCA CTGACTTAAA CCGTTTGTAA CACAGTTAGG AGGCCAAAAA CAAAAAACAA 600
AGCAAAACAA AACAAAAAGC AGGAAACAGT CTGTTAAGGA GCAAGGAAAA GAACAGTCCC 660
AGAGGCCGGG CGCAGTGGCT CAGGCCTGTA ATCCTAGCAC TTTGGGAGGC CGAGACGGGT 720
GGATCACTTG AGGTCAGGAG TTCTTAACCA GCCTGGCCAA CATGGTAAAA CCCCCATCTC 780
TACTAAAAAT ATAAAAAAAT TAGCCAGGTG TGGTGGCAAG CGCCTGTAAT CCCAGCTACT 840
CTGGCTCAGG CAGGAGAACT GCTTGAACCT GAGAGGTAGA GGTTGTGGTG AGTCGAGATC 900
ATGCCACTGC ACTCCAGCCT GAATGACAGA GCAAAATTGC CTCAAAAAAA AAAAGAAAAA 960
GAAAGAAGCA AAGAATAGTC CCAGAACCCT ACCTCTTTTT TTTCCCCAAA GTGTTGAGAT 1020
TACAGGTGTG AGCTATCGCG TCCAGCCCCA GAACCCTACC CTTTTTACTC CACAGAAGTT 1080
TGGAGTCTTA TACAGGCCTT CAAGCTGACA GACGAGTACA TACTAGCTTT TTGATTCTCT 1140
TCCAAATTCC TTAGTTATGA CTATACTTTT GGCAGTCTCC TGATAAAATA AAATCTACCA 1200
ATATATTTCA GTTCAATCAC ATGTTTGGGA AATACCTACT TCCCATCAAG TCTAAACTGC 1260
TGTAAAGGAG AATATAGGAA AAACAAATAA AACCAAGTTT CTACCCACAA TGTACTTCCA 1320
ATCTCGTTAG GGTACAAGAC CAGCTTGTAC ACAAGCTGTG TTATGTTCAC AAAAACAGCT 1380
AAGAAAAGAT AGTGCAGTAC TAATAAACGA GGATTCAAGT GATAAAATCA AATATTTGTA 1440
TTTGTTCATT TAACAATATT AACTAAACAC CTACTTTGTG CCTGGCAGTT ATTGGTACTG 1500
GGACTAAAGT AGTGACAAAA CAAAACAGAG CTAACAATCC AGTGAATGAA ACATATGTTG 1560
CCTAAGACAT ATGTGTACCA GTAGCATATG TTATATTTAC TTAGAACCAG AAACACAGTT 1620
GCAGGCAAAA GCAGTGAATA TAAAAATAAA CACAAAAAGC AACTGGATGC CTATTTAACT 1680
CTGGAGTCAA GTAGAGAACT GATGTTCAAC TTTAAAACTG CTTGCTTGCT TGCTTATTCA 1740
TTTATTTGTT TATTTATTTG AGACAGGGTC TCGCTCTGTT GCCCAGGCTG GAGTGCAGTC 1800
ATAGCTCACA GCAGCCTCGA AATCCTGAAC TCAATCAATT CTCCCGCCTC AGCCTCCCAA 1860
GTTGCTGGGA CTATAGGCGC ATACGACCAC ATGCAGCTGA TTTTAATCTT TTTGGTAGAG 1920
ACAGGGTCTT GCTATGTTGC CAGGCTGGTC TCGAACTCCT AGCCTCAAGC AATCCTCTCA 1980
CCTTGGCCTC CCAAAGTGCT GGAAATACAT GCATAAGCCA CTGCACCAAG CCTAAAAACT 2040
GTATTCTAAT CTGGTATTTA TTCTACAGCT AGTTTTACTT TTTTTTTGAG ACAGTCTCAC 2100
TCTGTTGCCC 2110
|
