| Tag | Content |
|---|
EnhancerAtlas ID | HS060-25934 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr4:3060070-3061330 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr4:3060268-3060285 | AAGGTCTTTGTGACCTG | - | 6.09 | | ESR2 | MA0258.2 | chr4:3060269-3060284 | AGGTCTTTGTGACCT | - | 6.63 | | IRF1 | MA0050.2 | chr4:3061305-3061326 | AGGTTGTTTCATTTTTTTTTT | + | 6.07 | | MEF2C | MA0497.1 | chr4:3061287-3061302 | TTCTATTTTTGGACA | - | 6.94 | | RFX5 | MA0510.2 | chr4:3060095-3060111 | TGTTGCCATGGCATCA | + | 6.12 |
|
| | 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 |
| GH04I003058 | chr4 | 3060206 | 3061524 |
|
Enhancer Sequence | TAGAACATAT AGGGTAACTT CTATATGTTG CCATGGCATC AGTAAACTGT CATGGGGCTG 60
GTGGGAGTGC CTTTTAGCAT GTTAATGCAT TATAATTAGC TTATAATGAG CTGTGAGAAC 120
AACCAGAGAT CCCTTTCATT GCCATCTTGG TTTTGGTGGG CTTTGGCCAG CTTCTTTACT 180
GCAACCTGTT TTATCAGTAA GGTCTTTGTG ACCTGTATCT TGTGTCAGCC TCCTACCTCA 240
TCCTGTGACT ATGAATGCCT AACCTCCTGG GAACGCGGCC CAGCAGGTGT CAGCCTCATT 300
TTACCCCGCC CCTATTCAAG ATGAAGTTGT TCTGGTTCCA ACGCCTCTGA CATATTAGCT 360
GCATCATTTT ACATTTCTTT TTTTTTTTTC CTTTTAAATG GGGTCTTGCT CTGTCACCCA 420
GGCTGGAGTG CTGTGGTATG ATCTCGGCTC ACTGCAATCT CCACCTCCGA GGTTCCAGCG 480
ATTCTCTTGC CTCAGCCTCC CGAGTAGCTG GGACTACAGG CACCCACCAT CATACTGGGC 540
TAATTTTTGT GTTTTTAGTA GAGATGGGGT TTCCCCATGT TGCCCAGGCT GATCTCAAAC 600
TCCTGGGCTT AAGCAATACA GCCGCGTTGG CCTCCCAAAG TGTTGGGATT ACAAGCATGA 660
GCTACCCCAC CCAGCTCATT TTACATTTCC ACTTGTTAAA CTGAAAACTG GCCCGAGAAA 720
GCTTCTGTAC TGCCATCCTT GCGTCCTTGC AGATGAATCG TAACCTAGCA TAGTAGGTAG 780
GCAGACTGAA AACCTAACTT AGCAGTAGGC TTCTGTAACA ACAGCTGTGT CTCAGCCAGT 840
TCCTGCAGCC AGACTTCAAC CACTCACAGG CCGCAAACTG TTCAAACTGT GTTCGGAGAA 900
GGCGAATTCA TCTGGCTGTT AACGTGCCTC ACTTCTGCTT TCTGTGGCCA CTTTCCCTTT 960
TCTGTCCATA AATTTGCTTT GACCACACAG CATCCCTAGA GTCTCCCTGA ATCTGCTGTG 1020
ATTCTGGGAC CTGCACCATT TGTGAATTGT TTTTTTTTTC CTTGATCAGC TAAACTCTGT 1080
TCAATTCAAT TTGTTGGAAG TTTTTAACAT ACCAATGGTG CACCAAGGTT CCAATTTCTC 1140
CACTTCCTCA TAAATAAGTC ATTTTAAATG GCTTTTCAGT ATTCCAATAT TTGGAAGTAT 1200
TAATGTTTCT ACCAATTTTC TATTTTTGGA CATTGAGGTT GTTTCATTTT TTTTTTCTTT 1260
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