| Tag | Content |
|---|
EnhancerAtlas ID | HS060-04706 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr10:111913010-111914480 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr10:111913038-111913050 | GGCCACGTGGCC | + | 7.22 | | MYCN | MA0104.4 | chr10:111913038-111913050 | GGCCACGTGGCC | - | 7.22 | | NEUROG2 | MA0669.1 | chr10:111914076-111914086 | AACATATGTC | + | 6.02 | | NKX2-5 | MA0063.2 | chr10:111913614-111913624 | CTCAAGTGGT | - | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CAGAGAGCTT GTCAGACCAT AACTCAAAGG CCACGTGGCC ACCATTGCCC ATTGACACTA 60
CCTCCGAAAC CTCTCTCCCG TTCAGCTCCT CTTTCTATCC CCATTGTCAC AGCCCTAGTC 120
TAAGCCCCTG GTTTCCCACC TGAATTCATT TAAACAACGA ATTCATTGAC CCTCTTACTG 180
GTCTTCCCAG TACCCCCTGT CTCAACCCTC AGTCCAGCCT CCCGCTGCTG GAGAACGAGC 240
TCTTTAAAAT GCAAATCATG GTCTGTCACT CACCGCCTAG TTGCCTATGA CTTGTGAGAG 300
ATGAGATCCA ACTTCCTTTG CAGGGAGAGA GTTCATTGGT GCCCTGGCCT TATCTGCCTC 360
CTGGCTTGGT TGCTACCCTC CCACCAGTCG CCTCATCTGC CACTTGCATT CACAATACTA 420
GGCCATTGCA CATGTTCTTT TCTCCGCTTG ACAGGTCCTT ACCCTGCTCA ACTGAGAGCC 480
AACTTCTCAT CCTCCAGGGA GGAAGGAGAC ACGCTATGTG GCAGGCACTG TGCTAAGCAT 540
TTTATTTGCA TTATTTCATG AGACAGATAC TATTATCCCC ACTTAGTGGG TGATAAAACC 600
AAGTCTCAAG TGGTTAAACA GAATTCAATC CTAGATCAAT TATGACCCTA AATCCATGTT 660
TTCCTGTTAC ATCTATTTCC CAGCTCAAAT GCCTCCTCCT TCATGAAACC TTCCCCCACT 720
ACGAGTGTGG AGGCCGGATC TGGCTTGGTG TTTTAGGGGA CAGAGTACAT AAATGAATTT 780
CAGAGATGCA AAAAGTTTCT GTTTAGGGGA AGTGCATGAT CAGTCCAACA AAGAGATTCA 840
GCATTTCCTG TATTCAAGGA ACATGTCTGG GTGCTGCACA GAATGAAACA TTAATTGGTG 900
GGCAATAACG TGTTGGCAAA GACATGGAGA AATCAGAGTC TTCATACATT GCTAATGGGA 960
ATGTAAAATG GTACAACCAT ATTTGAAAAA CAGTTTGGCA GTTCCTCAAA AAGTTAAACA 1020
TAGAGTTACC AATTCTACTA CTCAGTATAT ACCCAAGAGA AATGAAAACA TATGTCCACG 1080
TAAAAATTTT CACACAAATG TTCATAGCAG CATTATTCAT AATAGCCAAA ATCTGGAAAC 1140
AACTCAAATG TCCATCAACT GATGAATGAA TAAACAAAAC ATGGCATATG CATTCAAGGA 1200
ATATTATTTA GCCATGTAAA GGGATGAAGT ACTGATACAT GCTACAACAT GGTGAACCGT 1260
GAAAACACTG TGCTAAGTGA AAGAAGACAC CTATTGTAAC ATTTCATTTG TATGTGAATG 1320
TCTTGAGATG TCAAGAATAG TAAAAATCAG CCAGGTGCCA TGGCTCATGC CTGTTATCCC 1380
AGCAGTTTGG GAGGCTGAGG CAGGTGGATC ACTTGAGGTC AGGAGTTCGA GATGAGACAA 1440
GCCTGGCCAA CAGGGTGAAA CCCTGTCTCT 1470
|
