| Tag | Content |
|---|
EnhancerAtlas ID | HS048-19705 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:10212750-10213990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr2:10212873-10212892 | TCACCACCAGAGGGCACTG | + | 7.86 | | KLF4 | MA0039.3 | chr2:10213496-10213507 | ACAGGGTGTGG | - | 6.14 | | ZEB1 | MA0103.3 | chr2:10213058-10213069 | GCGCAGGTGGG | - | 6.62 | | ZNF740 | MA0753.2 | chr2:10213336-10213349 | CCCCCCCCCCCCC | + | 6.03 | | ZNF740 | MA0753.2 | chr2:10213337-10213350 | CCCCCCCCCCCCC | + | 6.03 | | ZNF740 | MA0753.2 | chr2:10213338-10213351 | CCCCCCCCCCCCC | + | 6.03 | | ZNF740 | MA0753.2 | chr2:10213339-10213352 | CCCCCCCCCCCCC | + | 6.03 | | ZNF740 | MA0753.2 | chr2:10213333-10213346 | CCGCCCCCCCCCC | + | 6.64 |
|
| | 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 |
| GH02I010072 | chr2 | 10212801 | 10213010 |
|
Enhancer Sequence | TTTGGTTTGT TTGGCTTTTC GGTTTTCTTA AGGAAACTTG AACATGTACA GTAGAGAAAC 60
TCCTACAACG GCTCTCCTGG ACCTGACCCA GCTTTCACAA TTTTGCTAGT CTCGTTCTGT 120
TGCTCACCAC CAGAGGGCAC TGTTCTCCCC ACACAGAGGC CAAGATCCCA GTGCCCTGGG 180
GAAGCTCCAC TGTAGGGCTT TGCAGGCAGC AGAAGCTGAG CAGTGCAGGT GGAGGAGCGG 240
TGGGGGAGCG GTGCAGGCAG GCTGTGAGTC GGAGAGTGGT GCGGGTGGGC TCTGCGTAGG 300
GGGGGATGGC GCAGGTGGGG TCTGCGCGGG GGAGCAGTGC AGATGTGTGG GAGCAGAGCA 360
GATGTGTGGG AGCAGTGCAG ATGTGTGGGA GCAGAGCAGA TGTGTGGGAG CAGAGCAGAT 420
GTGTGGGAGC AGTGCAGGTG GGCTCTGCAT GGGGGGGCGG TGCAGGCTGG CTGTGTGGGA 480
GTGGTGCAGA TGGGCTCTGG GGGGCAGCGG TGCAGGTGGG CTCTGCGATG AGACCTGTCT 540
TGCATGGCTA ACATGACAAG GACGTGACAA GGGGCTCTGG GAACCGCCCC CCCCCCCCCC 600
CCGGCTGTGG GCTGCCAGTC CAGGGCCCGT CTCCACTGGG AAGGCCTTGC CTTGAAGGAG 660
GTGTTTCCAA AGCCACAGGG AAAAAGGCAA GGGAGACCCA GAGAGGCTGT CACTGGACTC 720
AGGGTCTGAG AGACTTGTCC GTGCTAACAG GGTGTGGATT GCGGTTGGCC TGACCTGCAA 780
ACAGGCACCC TCCCACTCCT TGCTGGGCCC CAAAGTCCTC CGATGTAAAT AAGAAGGTGG 840
GACTGAACCA TCTGTGAGGT CCCTTAAGCT CAAGTCATCT CGGATTTCAG CAATAGAAAG 900
AAATGACAGC TGTCTGGCCA TATACTATCA AGAAACAGAG CTTGGTGGGA ATCGGAATGG 960
GTGGCCTTGG GCAGGGGGCT GCTTTCCCTG CTGGGTAATG GGCTCACGGC ATTTAGGGGC 1020
AGAAGGGCCT GTGTTGTGCA CAAACCACTG CTCTGACCCT CCTTCCCAGA GTCTAGTTAG 1080
GGTCTGCCCC AGCCCTATGG GACTCAAAGC TCCAAGGTTA AGAGCTCTTG GTCAGCATCT 1140
CTCGAAGAGT GCATGAGCCG ACATCCTCCT TTCCACGGCA TTTCTACACC CTGCCGTGCC 1200
CAGTACTCAG CAGCAGCCAC CACAGCCTCT CAGCAGGGCA 1240
|
