| Tag | Content |
|---|
EnhancerAtlas ID | HS105-62816 | Organism | Homo sapiens | Tissue/cell | IMR90 | Coordinate | chr4:184910460-184911620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HES2 | MA0616.2 | chr4:184910497-184910507 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr4:184910497-184910507 | GGCACGTGCC | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr4:184910573-184910588 | TGAACTTCTGACCTC | - | 6.38 | | RARA | MA0729.1 | chr4:184910570-184910588 | TCTTGAACTTCTGACCTC | - | 6.88 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TTCTTCTGCC TCAGCCTCTT GAGTAGCTGG GATTACAGGC ACGTGCCACC ACGCCTGGCT 60
AATTTTGTAT TTTTAGTAGG GACGGGGTTT CTCCACATTG GTTAGGCTGG TCTTGAACTT 120
CTGACCTCTG TTGACCTGCC TGCCTTGGCC TCCCAAAGTG CTGGGATTAC AGGCGTGAGC 180
CACTGTGCCC GGCCTCGACA TTTTTTCTTA CCAATTAATA TATAGTGCCC GAAATTTTGC 240
ATACTGTTTG GCCTGTTAAC CTACATGCAA TGCACTAAAA TCCAAGAAAG CCTGATTTAT 300
GTGCCCAGGG ACTGTTTCCA AGACTAACAT CATATTGAGG CTGCTGTTAA CTGCTAAGGA 360
AGTAAGCATA TTTCATCATA GTCTGCTTTA GGATTCAGAT TATGACAGAG CTGTTTTCTT 420
ACAACATCCA TGGGCTTTTC ACACGAAAGC TTTTTAAAAA AACATGACAA CGAAATGGTA 480
AATTTTGGTC CTCAAAAGTA CATTACATGC CTCATTTCCA AAGTGAGACT TGGCACATCT 540
GAAAGCATGG CTTTACCCCC TCATCACATG GATGGTTTCA GCACTGTTAC AGATATTTCT 600
GAGAGTGTTG AATCCCGTAT GTAATAGGTA AGAATTTTTA GAACATGTTT AAAGGCAGAT 660
GTTCAAGACC CCTTGAACAT CTTCTTTCTC TTCGCAGTCA CATCCATCTC ATAGCTCACC 720
CTGTCACAGA AGAAAAGAGA GCATGTTTCC TTTCTCCACT GTCAGAGGTC TCTTCTTTCT 780
GCATAGCAGT TTGCATCTTC AGAGCAACGT TGAGGATGCT GAGTCAGGTT TAAAGGATGT 840
TTGGTCAGAA AAAACACAAG CATGGTATGT TGCAAATACA GTTCCATCAT GTCCTCACAC 900
CCATCAATTC TACCCATCCT TAAGGACCTA TTCCAAATCT CTGTCCCCTG GAAAGTTCTC 960
CCTAATCACC CCAACAGGAG GTCATTTCTA AATCCTTGAA ACTCCCATTA TAGAGTTAAG 1020
TTTCTATTCA TTCATGTGTT TTCTTGCTAT AGCTCTTCTA AGGGTGTTTT GAACAGCAAT 1080
GTGTATATTT CATGATGCTT TATATTTTCA CACATGTATA TCTTATATTC CCACCTAAAT 1140
TGTAATCTCA TTGAAGGCAG 1160
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