| Tag | Content |
|---|
EnhancerAtlas ID | HS095-00608 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:27353460-27354410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:27354351-27354361 | AATGGAAAAT | - | 6.02 | | SP1 | MA0079.4 | chr1:27353734-27353749 | TAAGCCACGCCCCAC | + | 6.16 | | SP4 | MA0685.1 | chr1:27353734-27353751 | TAAGCCACGCCCCACTC | + | 6.28 |
|
| | 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 |
| GH01I027026 | chr1 | 27353011 | 27355170 |
|
Enhancer Sequence | CAGGCTCATT TATTTAATTT TAGTCAACAT CTCTACTTTC ATGTTTGTAG TCATCTCAAA 60
TTTTGCACGT TCAATGTTGA CTTCTCGAAC TGAAGTCCTA GCAAATGGCA AATTCCAGTT 120
CTTGGCCCCA AACTCTGAAG CCACTTTCCA CTCCTTTTTC TCTCACGCTG CACTTTCTCA 180
TTCGTCAGCA AGCCCTGTGG CTCTGCCTTC AGAACCCAAA CAGGCCCTGA CCACATCTTG 240
GCCCCACCTC CAGCTTACTG CCATCTCTGC GGTCTAAGCC ACGCCCCACT CTCCAGGATT 300
TTTGGAGCCT TTCTGCCGTC GTGCTTGTCG CCTACAGTGT TTTCATCCCA GCAAGCCAGT 360
GTGATCCTTT CTAAACACAA GTCAGATCAT GTCATTTTAA TGCCTCCTTC TCATTTGGAA 420
TACAAGCCGA AATCTCCTCC CACACCCCTT CCCTTATCGG GGGCAGCCAC ACTGGCCTCC 480
CTGATGTTCC TCAACCATGC CAGGCACGCT CCCACCTCAG GGCCTTGCGA CTGCTCTTCC 540
ATCTGCCTGG CACGGTCTCC TTTGATCCCC ACATGGCTGC TCTCTCAATT CCTCCAGGTC 600
GTCTTCTCCA TGTCTCCTGT TCTCAGGGAG GCCTTCTCTG ACTATCCAAT TAGAATGGCG 660
CCCTCGCTCC CCACACCTGC TAGCCTCTTC TCTATTTCCA AAGCACCTAA CACCATCTAC 720
CATGCTGCGT ATTTACCTAT TTATTGCCCC ATTTCCCGCC CCTGGAACCA AAGCTCCAGG 780
AGAGCAGGGA TTTTGTTTTC TATGTAATCC AGCACCTGGA AACCTGTGTG TGCTCAGTAA 840
ATATTCACGG GATGAGTGAA GGTGAGACAG GACTAACATG GGTCGCAGAA GAATGGAAAA 900
TTCCAGGCAG CAGTTTCACA TGACTAGCAA AAGGAAGCTG TTGAAATAAC 950
|
