| Tag | Content |
|---|
EnhancerAtlas ID | HS048-20592 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:70202540-70203680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MYCN | MA0104.4 | chr2:70203302-70203314 | GGCCACGTGGTC | + | 6.52 | | MYCN | MA0104.4 | chr2:70203302-70203314 | GGCCACGTGGTC | - | 6.52 |
|
| | 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 |
| GH02I069974 | chr2 | 70201673 | 70207660 |
|
Enhancer Sequence | TGCTGCTCCT CCCCCGAGAA GCTTCCCTGC CTCCTCCCAT GTACTTCAGG GAACTGGTAA 60
GTTTGGAAAG CACCCAGAAT TACTTGAGGA AAAGACTGTA GCAAGTACAA TTTGAATTTG 120
CCAAGAGACT TTGCCACCAA ATTCACTTGC CTAGAGAGAG AGGCGAAGTC CATGGGTTTC 180
TCCCTGTGGT TCTGTGGCTT CACCGGGAAA ATGTGGGCCT TGCTGAGCTA TGGAGGGGAA 240
AGGAAAGGAG CGTGAAGGAG ACAGGAGGCA GAAGCTCCTC ACAGTGCCCA GCACGCAGTA 300
GGGGCCGAGA TGATGTGCTG AATGATGGGC CTCATGGCCA TGTGAGTGGA AGGCCAGGCA 360
GAGCTGCTTG TTTAATATCT CCTACTCTTT CCCCCGTGGT CAGTGAATTT GCTTTTGGTT 420
TTGAATTTGC TTTGGCTGAA CCAGGGACAA TTTCTACATG GCCTTGAGGC CACAGGCATA 480
TGTAGTCAAC TGCACACCTC AGGGTGCAAG GGGTTACACC TGTTCCTTGC TCAAAAGTCA 540
TGGGAAGTTG CTAAACAGAC CAAAAGAAGA ACCAGCACGC TTACTGCTCT CCGTCCTCCC 600
CTTCCCCACC CCACCCCCAG CTGTTAGCTC ACAGAGGGTC AAAACAGGCA AGATAAAATC 660
TGTCCAACTC ACAGCTTCAA AGGAACACAA GTTAGACATG TGACCCAACC GCACCCAGCC 720
TTGTCCCTCC CAGGTGCATG GCCCTGGAAG GCCCAACCCT CCGGCCACGT GGTCCGTGTA 780
GAGGCCAGGT GGGCAAAGCC TTCCGTTCCA GACCCAGTGC TGCCCTCCCA TGAGATCCCA 840
ATCTGATTTT GGTCTTCTTG TAGTTCTCCT TGGAAGCCAG GCCCAGCCCC ACACTGCCTC 900
CTCCTCACGC TCACCTGGCT CCCTCCAATC CGATCTGGGG CAGGAGGCGA TGCAGACCGC 960
AGTCTTCACC GCAACCTCGA CCCTGAGGGC CCAGAGTCAG TGCTGGAGCC ACCTACCAGG 1020
AGTCACTTCC ATAGCCCTTG AGGCTGAATG AGAGCCCTCG GGTTCTTGGA TAGCAGAGAA 1080
CACAACCCAG ACATGGCTCT GGATATGAAA CAAATCCTTT CTGAACCTGA CACCAGACTT 1140
|
