| Tag | Content |
|---|
EnhancerAtlas ID | HS184-30821 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr9:33220670-33221830 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr9:33221449-33221464 | GGGTCAGGCTGCCCT | - | 6.02 | | ESR2 | MA0258.2 | chr9:33221449-33221464 | GGGTCAGGCTGCCCT | + | 6.36 |
|
| | 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 |
| GH09I033221 | chr9 | 33221061 | 33222377 |
|
Enhancer Sequence | GTGGGCTGCT GGAAGACAAG TTGAGTCCAA ACTAGCCCAG TTCTTGAGGA GCAACCACGT 60
GACTCTATCA CCGTGATATG CACAGGTTGT GACTGGTGTC CTCAGACTGG AAAACACAGT 120
AGTGCCAGCT CAATCAGGAT AGGAGAGAGA CGTATACGTT GACATTTGTC TTCCTATCCG 180
GATGAGTGTG GTCCTGCCTT TGGGCCTTTC CTTGGGCCCT CCCCTCTATG TGAAATGCCA 240
TCTCTACTAG CGAGATTCCT GTCTGATTTA TTTGTTTAGG TAGAATAGCA AGAAGTCTAC 300
ATCCTGATGA TCCTGGGCAT TGGGAGCTCA CCTCACCTTC TCTGGACTCT GGAGGGCACA 360
CACATATGGT CCCTGCTGGG GGATGCTTCG CACACAGACC GTCTTCCAGA GGCAGGGGCA 420
GGGAAACTGC TGTCAGGTGG GTGTTGGGAT CTCTTTATAT TTAGTTTTGT TGTGCTGTGG 480
TTATTGATGT TGCGGTTTTC AGTTTCCTTC CCTCGTAGTT ACTCCCCACC TGGGCTAGCC 540
ACTCTCTACC CATCACAGGC CCAAGTCTGT GAGAAGGGGC TTCTCTTAGG TCCTCACCAA 600
GGCCCCTTCC CAAGGTCCCT TCCCAAGGCC CAACCTGCCC ACAGTCTCAC CGAGGCCAGC 660
AGGGCCCAGG TCTGGGCCCA GGTCCAGTCC CAGGCAAGGG TATTGTGTGT GCTTCCTGAT 720
AGGTCAGGCC GCCCTGAACC CTCCAGGCAC ACTGGCCCTA AATGTGTCTG CTTCCTGAAG 780
GGTCAGGCTG CCCTGAACCC TCCCTGCGCT TCCTCTTGTG ACCAGTGTTG AAGATCAAGA 840
GGAAGAGGAA GAGGCCAAAA ATTCTTCACA CAGAGCCCTG GGCTCCGAGC CCCTGTGGCC 900
TGTCACTTAC CTGGTCCACA GCAGAGGTGG TGTCTCTAGA TGAGGGTAAT GGGAAGCATC 960
CTTCCCTCAT GCCCTGCTCC CTTCCTCCGA GCCATACCCA TTACACTGAG CCAGTCACGG 1020
CAGACATCTA GGCAGAAGGG ACCACAGGGG TGGCCTCGTT GCCTGTCCTT GCTCCCTCCA 1080
CACTGCATAT CTGCAGTCTA ACCTGCTGAA TCACAGTCCT TGTTAGGTGA GGGCCAGGAC 1140
AGGAGAGAAG ACACTTCACT 1160
|
