| Tag | Content |
|---|
EnhancerAtlas ID | HS048-20659 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:73912750-73914110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:73912902-73912920 | CATGCCCTCCCTCCTTCC | - | 6.37 | | NFYB | MA0502.1 | chr2:73912861-73912876 | CTGATTGGTCCAAGT | - | 6.77 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 73913200 | 73913580 | | chr2 | 73912886 | 73912957 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I073685 | chr2 | 73912747 | 73913897 |
|
Enhancer Sequence | TTACAATTTT ACCAGGTTCA GAATAAAATA CCATCCTTCA AAATGAACAA ATTACTTATT 60
AGCCGAAGAA AGGTGAAAGG AAGTTTGGAA TTAACAGTCT AGATTTTCTC ACTGATTGGT 120
CCAAGTCACT GACCTCTAAA ATTATCTTAG ATCATGCCCT CCCTCCTTCC TACTTTCTGG 180
AAAACAATCA GTCTCCTACC CTATGCTTGC CCAAAGAGTT TCCCATACAA ATCACAAATC 240
TGCACTTGCC ATTCCCTGGA AGCCCTTACA TTCCCAAGGC CTGGCCTCAT CCACTGCCAC 300
TGCCCATGGC CCCAGTCCAG GCAAAGCAAT CACTCCCTCT CCCTCTCTGT CATTCCTTTC 360
TTTTCCTTTC ACTCTCTTTC TACCCTCCTC TTCCCCACTC TCTGTTTCCT CTCTCTCTCT 420
CTATCTCTCT CTCCCCACCA TCTCCTCTCT CTGTCTCCCC CCGCCTTCTC TCTCTGTCTC 480
TGTCTCTCTG TTTCTCTGTG TCTCTCTCTC TGTCTCTCTC TTTGTCTCTC TCTCTGTCTC 540
TCTCTCACAC ACACACACAC ACACACACAC GCACACACAC ACACAGCCAG CAACATTCTA 600
CCTCTGCCAG AGTTCCAGGT TGAATAGGTG TGGACTTTGA CTTTCAGATT CCTCTGGCAA 660
GTGTCAACAT CAGTCCTGTT GCTCCCTGGC AGAGGAGGAC TTGGAGTCAC CTTGGCCAAG 720
AAGCTGTCTG GAGGTCACAG TGGCACCGCC CATCGGCCCC TTGGCTGAGG CTAGATGAGG 780
GCAGATTCAG CACAGCAGCA ACTCTCCCCA TAAAAAAAAT CCCTCAGTGT CTTAGTTCTC 840
TGACCCTTGT ACTCCTTGTG AGTTTTAGAG CCACATGAAC TCTTCTTTTT TCCCAATGCT 900
TGGAGACAAA ATTTACATAA CCTACAGTTA GCCATTTTCA AGTGTACAGT TCCCTGCCAT 960
TTGGTACATT CACAGTGTTT TGCAAGCAAC ACCCATATCA AGCCCCAAAA CATTTTCATT 1020
ACCCAGGAAG GAAACCTGTC GTCATGGAAC CGTCACTCCT CACATCCCCT TCCCCTCAAA 1080
CCCTGGCAAC CCCAAACCGT TCTTGACAGC CTCCTTTGGC ATTTCTTCAT TTTGGTGTCA 1140
GATCTCACAG CAGAATTTCT TACCTATTAT ATCCAGTGCC TCAGTGCGAA GTTCCAGTTT 1200
AACTTCCTGT TACCTCGAGC CCACTATCTT GCCCCAATAA TACCCTCCCC CAATTCACAA 1260
ACACAGACGC ATTCCCTCCT ACAGCTTTGG GCCTCCTATC TGAGTCCTTC AGGAAAGAAG 1320
AGCTTGTAAC TCCCTTAGCA GTGAGTGTAG ACTTGGTCCA 1360
|
