| Tag | Content |
|---|
EnhancerAtlas ID | HS095-22299 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:25322200-25323610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:25322579-25322597 | CTTTCTTTCTTCCCTTCC | - | 6.03 | | Foxd3 | MA0041.1 | chr4:25322996-25323008 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr4:25323000-25323012 | GTTTGTTTGTTT | + | 6.32 | | Nkx2-5(var.2) | MA0503.1 | chr4:25322225-25322236 | CTTGAGTGCTT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr4:25323213-25323228 | TGAACTCCTGACCTC | - | 6.22 | | TCF7L2 | MA0523.1 | chr4:25322569-25322583 | TTGCTTTGAACTTT | - | 6.03 |
|
| | 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 |
| GH04I025320 | chr4 | 25321995 | 25323461 |
|
Enhancer Sequence | GAATAAGGGG GGAAAGCTGA GTAATCTTGA GTGCTTCATA TTCTCATGTT CTCTCTACCA 60
ACCTTTTAGA AGGCCATGTG TCTGAATGTT AAATTTAAGG CATAATAGTT GCTGATTATG 120
TTGTGATTTT GAATAGAGAG AAATATGCAC AAGATCTCAG TTTATCTTTT ATCAAGAAAA 180
GGTTAATAAA CTAGCAGTGA AGCTTTCTGA AGGGCAGTTT GGAAATATTT AAAGGAAAGA 240
GTTAATTGAC AAGGCACAAA GATGTATCAT GTAAGTGGAG GTTCATTTTG CAGTGTTCTT 300
TTCCTTCTTT TAAAAATGAT TAAACTCAGC TCCTTATGGT GAGTGAATCA TCACCACATC 360
AGCCCCTCAT TGCTTTGAAC TTTCTTTCTT CCCTTCCTAG TGATTTTGCA ACTTCTGCCT 420
TCAGCTAGTG TTACTCAGTG GGTGATAGGT AGTCCTTTTG ACCATATTTG AGTAACAAAA 480
CCCGATACAA CTTCCTCTAC TTGTGGGATT TTCCTTTCTT AGGTCCTCTA AAGGCCTTAA 540
TTATTGTTGT TATTCTTTCA ACCAGGTATA TTTTTTCTTT CTTTTCTCTG TCTGTCTCTT 600
TCTTTCTTTC TCTCTCTTTC ACTCTTGCTG CCGCTCTTTC TTCCTTTCCT TTTCTTTCTT 660
TCTCTTCTTT CCTTTCTTTT CTTTCTTTTT TTGGAGGCAG AGTTTCATCT GTTGCCCAGG 720
CAGGAGTGCA GTGGTGCATT CATAGCTCAT TGTAGCCTCC AACTTTTGGG ATTAAGGGGT 780
CTTCCTGGCT AATTTTGTTT GTTTGTTTGT TTGAGATGGA GTCTTCCTCT GTTGCCAAGG 840
CTGGAGTGCA GTGGCGTGAT CTTGGCTCAC TTCAACCTCC ACTTCTGGGG TTCAAGCGAC 900
TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ATTACAGGCT CCCGCCACCA CGCCCAGCTA 960
ATTTTTGTAT TTTTAGTAGA GACAGGGTTT CACCATGTTG GCCAGGCTGG TCTTGAACTC 1020
CTGACCTCAA GTGATCTACC CGCCTCAGCC TCCCAAAGTG CTGGGATTAC AGGTGTGTGC 1080
CACGGCGCCT GGCTGGCTAG TGTTTTAAAA TATTTTTAGA GATGGGGGTT CTCAATATAT 1140
TGCCCAAGCT GATCTGGAAC TCCTGGAATC AAGTGATCCT CCTGCCTCAG CCTCCCGGGT 1200
AGCTGGGATT ACAGGTGTGA GCCACAGTAC CTGGCCAAGG GATATTTACT TCTCTGATAT 1260
CAAATGCATG TCCTGTTGCT CTGTTCTGGT GGCTGACTGA AAGTACATGA TATGTTTCAG 1320
TAATGAATCA TAGGGTGATG GCAATTAACT CTCCACCTGT AGTTCCAGCC ATGCACAACA 1380
CTTGCCTGAA GACATGACAG CTTCAAGAGC 1410
|
