| Tag | Content |
|---|
EnhancerAtlas ID | HS007-09897 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr2:242697820-242699350 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ONECUT1 | MA0679.1 | chr2:242698453-242698467 | ATTATTGATTTCTT | - | 6.29 | | ONECUT2 | MA0756.1 | chr2:242698453-242698467 | ATTATTGATTTCTT | - | 6.36 | | ONECUT3 | MA0757.1 | chr2:242698453-242698467 | ATTATTGATTTCTT | - | 6.52 | | ZBTB7C | MA0695.1 | chr2:242699182-242699194 | GTTGGTGGTCGC | - | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 242698604 | 242698741 | | chr2 | 242698564 | 242698745 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I241759 | chr2 | 242698564 | 242698745 |
|
Enhancer Sequence | TTTTCCCATA TTGGCATAAA GTTGTTCGAA TATTCTTTTG TTGTCTTTTT ATGTAGCATT 60
TGTGGGATGC CCCCACACCC TTTTTTTTGG TGGGGACAGG GTCTCGCTGT CACCCAGGCT 120
GGAGTGCAGT GGCTCACCAC AGCCTCGACC TTCTGGGATC AAGCAGGCCC GCCACCTCAC 180
ACACACCAGC AGGCCTGGCT AACTAAAAAA AAATTTTTTT GTAGGCCCGG TGCAGTGGTT 240
CACGCCTATA ATCTCAGTAC TTCAGGAAGC CAAGGCTGGA AGGATCACTG GAGTCCAGTA 300
GTTCTAGACC AGCCTGGGCA ACACAGTGAC ATCTGATCTA TACCGCCCCC CGCCCCACAA 360
TATATGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTG TGTGTGTAGA GCCAGACTCA 420
TGTAGAGCCA GTTGTGTGGC CGGACCGGTC TTGAACTCCG GGGCCTCAAG CAAATGCTCC 480
CTCCTTGGCC TCTCAAAGCC AGAGATTACA GGCGTGAGGT ACTGTGCCTG GCATTATTTG 540
CTGCTTGCAT TATCATTCCT TCTTTGACCG ATGAGTTATG CAGAAGTGTG TTTCTTAATT 600
TCCAAACGTG GTGGTTTTCT AGTTATTTTA AAAATTATTG ATTTCTTTTT TATTGCATTA 660
TACCCAGGAA ACTTCGTCCT TATCAGATCA GATTTTTGAA ACTTGATCAG TGGCAGCTTA 720
TGATCAGCCT TCGTAACTGT GGAGTGCTTG AAAAGAATGT GCTCTCTGCA GTTGCTGGAA 780
TCAGTGTTTG TACAGATCCA TCAGATAGAA GTATACGTCG CGTGTTCATT CTACATCCTG 840
CTGACCTGCC ACTCCCTGAG GGAGGTGTTA GAAATCTGCT GACAACAGAC TAATCTGTTC 900
CTCCTGTAGC TTTGCCAGTT CTGGAGACGT GTTCTTAGGG GCATAGGACA TGAGGTTCGT 960
CTCTTTGTTT TGGGAAACTG AATCTCCTAA CGCGATGGAC TCGCTCTTTA TCTCCAGCAT 1020
TGCCCGCTGC CTTGGTGTCT GCTTTGTTTA TTACACAGTG ATGCTAACTT TCTTTTATTT 1080
AGTGTTTGCC TGATGTGTTG TTTTTCCTCC GGTTAGCTTC AGCTTTTCCA TCCTTAGTGA 1140
TTTAGATGTG TTTCTTGTGG ACGCCCCCGG ACAGGTTTCT TGCGTACTTG TTTGCCGTCT 1200
TGAATGAGAG CGTTTGGCTG CTGAGCACGT GCTGTGGCCC ACTGTTTGGA TTTGTCTACT 1260
TCACCCTGCT CTTTGTCTCT CACTTCTTGT CTATTTTTTC CTCTGTTTTT TGCTCTTCTG 1320
GTTTATGTTC TTTGTCATTT AGCTTTTTGC CGTTTACTAA CTGTTGGTGG TCGCCCTGGC 1380
ACCACAGTGG ACATTTCTAG CCCTCTGGGT TTGAGGTTAA TCAGAGTCAC TATCTTCCTC 1440
CCAAATAATG TGTGATGGTG AATTCTCTGC GTCCACTTGT CTGGGCCCTG GTACCCTCGT 1500
TTGGTCAAAC TCCAGTTTGG ATGTTTCTGT 1530
|
