| Tag | Content |
|---|
EnhancerAtlas ID | HS048-21867 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr2:201621220-201622590 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr2:201621320-201621338 | GGAGGGAAGGTAGGAAAG | + | 7.27 | | NEUROG1 | MA0623.2 | chr2:201622073-201622083 | GACATATGTC | + | 6.02 | | NEUROG1 | MA0623.2 | chr2:201622073-201622083 | GACATATGTC | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_35011 | chr2:201619028-201622689 | HeLa |
|
| | 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 |
| GH02I200754 | chr2 | 201619368 | 201623213 |
|
Enhancer Sequence | CCTTCTTGTT ATCTCACTTT TACAGAAAAC AGTGTCCTCT ACTTTAAACA TCCCCATCAA 60
CAGGATCACC TGTCATGTAA AACGAGTGGG TGGAGGTTTT GGAGGGAAGG TAGGAAAGCC 120
AGCTGTATTC GGGGCTATTG CAGCTGTGGG TGCTATCAAG TAAGTATGGT TGGGGATGCT 180
TAGGGATACA GAATGGCATC AAATGCACAG AGCTGAGGGC AAATCAGTGG CTGACAGTCA 240
TCTGGGCTGC CATCATAACC ATGTGTGTGT CCTTGGGCAA TTCAGCCTCC TGTCTGTTTC 300
TTTAAAAAAT GTAAATAATC ATACCTACCC TCCCACACTT TTAGAGTTAT TGCAAAAGTC 360
AAATGTACAC AGGACTTTGA ATAGCTGACA TGCTATTGAA AGGAGCAGTG GTACTATTAG 420
CTGAATACCT CCTGAGCTTC AGGGAAAGTG AGCCGTTGAG GGGTGGGGCA AGTCACCCTG 480
CCCAAGTGGA GTGCTAGGGG AGGCTGCTCC CTGACTCTTC TTTCCTGCTC TCAGACCAAG 540
AACAGGGTGA GGTAAGGAAA GAAAGGCTCT TCATCCTCTG CCTCCCTGCA CCTGGGAAGG 600
GCTGCGTCCT CAGAGTCTGC TCAATGGACA GATGACTCAT CCTCAAAGAC AGCTCCCAGG 660
CTGACCTCAG CGGAAGGCTC ACTCCTTTGC TGTTCATGCC TCAGATTTGT ATTTAGTTGG 720
TGCTGCTTTT TCTGTTAATG GTTCATTTTC TGTGGCTAAG TATTCTGTCA GAGCCCCAGA 780
GGGCATGCAA AGTTTACAGG CCCTGCTTCA TTTGACAACT CTTGTAGTTC AGAGCTAGGT 840
CCTGAAACAC TCAGACATAT GTCTCAGTCC TCAGTGAGAA GTGGGAAAAA GCAGGATCTG 900
AATCCCATCT CCAATTCTTT CCATAATTAA ATCCACTCCA CTCACACCCA CTGGGGATTC 960
AGCACAAGAT AATCAGTTCA TTGAATTCCC CCCAGGCGTT GTGGCTTTAA GACTTCTCAA 1020
ACACGACTGC ACGTTAGAAT CATCTGGGCA GCATTTAAAT ACCAGTGCCC AGGCTGCCCC 1080
ATACTGACCC AGGCATCCGT ATATTTTAAA ACTTCCTCAG TGGTTCCACT GTGCAGCCAA 1140
GTGTGGCAAC CAGTGCCTTA AGATACAACT CTACCTTGGT ACCCAAGGGC CATGCATTAA 1200
ATGATCCCCA GAGTAATGTT CCCAAACCTA ATAGTAAGTA AGAGTTGCCT GATGTCATAG 1260
AAATTCCTGC CTCAGCTGGG CATGGTGGCT CATGCCTATA ATCTCAGCAC TTTGGGAGGC 1320
TGAGGCAGGA AAATCACCTG AGCCCAGGAG TTCAAGATGA GCCTGGGAAA 1370
|
