| Tag | Content |
|---|
EnhancerAtlas ID | HS197-16195 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr4:124475440-124477630 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RARA(var.2) | MA0730.1 | chr4:124475636-124475653 | GGGTCAGTTGGAGGTCA | + | 6.39 | | ZNF263 | MA0528.1 | chr4:124477425-124477446 | CTCTCCCCTTCTCCCTGCCCT | - | 6.04 | | ZNF263 | MA0528.1 | chr4:124476003-124476024 | TCTCCTGCCCCCTCCTCTTCC | - | 6.34 | | ZNF263 | MA0528.1 | chr4:124476000-124476021 | TCTTCTCCTGCCCCCTCCTCT | - | 6.46 | | ZNF263 | MA0528.1 | chr4:124475993-124476014 | TCCTCTTTCTTCTCCTGCCCC | - | 6.92 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28360 | chr4:124473516-124479149 | Fetal_Intestine | | SE_29079 | chr4:124473558-124479050 | Fetal_Intestine_Large |
|
| | 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 |
| GH04I123552 | chr4 | 124473649 | 124479255 |
|
Enhancer Sequence | CAGGAGAGGG GGAAAGAGAT GAAAAATGCT GTGCAAAAGT TCTGCATTAA CAATGAGAAT 60
AAAAAACCTG TGGGAACCTC CCTCAAAAAT GACAGGGCTA ACCAGGAGTG CCCTAACTGC 120
AACTTTGCCC AATAGCATTT TCTTTTTTTT TTTTTGAATT GTGTGGTGTT CATTGACTGT 180
TGATTATTAC AGAACTGGGT CAGTTGGAGG TCAGGGAGGC AGGGAAGGGG TAAGCTGTGG 240
GCTGAGAGAT GAAACAAGCG GTTCTACCAA TCCATGTGAA ACCTTTAGGG AGAATGTAGG 300
GCTTTAAAAA ACACATTTGG GAAATTTTCT TTATAAAATT ATCAGAAGAG TAGATCACTG 360
CCCTGTTTAC ACTTTGCATA TGCAACAATA CAAATGTAGA AAAATAACCC ATTATGAGAA 420
AGCAGTGAAA ATAATTGCAC ATTAAGAGAG TTAGGTCACT GCTGGCCAGA TCTGGCTATG 480
ATTTGCATCA GTTTTAGTTT TTCCGAAAGG AATGTTTGAT CCAACAGAAA ATGGGCTTTG 540
AGTGTGCCAG AGCTCCTCTT TCTTCTCCTG CCCCCTCCTC TTCCCAGGTT GACGATGGAT 600
CCCCCAAGGC ACTTGTTGCT TCCTCCAAAG GAGCTCCCCA TTACAGCTGG AAGAGAGGCT 660
TGTTTCTCCA GCTGTCTAAC CTTTAGTTTT ATCTGCCTCT TGTTGACCTC TTAGTTTTAT 720
AATGAGTCAG TTTATTTGCT TGTACAAATT GAGTTTTCTT AGAAATATAA CAGTTAGAAA 780
GAGGCCAATG TTTTGTTTCC CCTTATGAAG GAGAAGTAGC TATGGGACCG GGCACGGCTG 840
AGGCTGTTCA TTCCATGCCA GTCCCTGTTG TTGGTTTATT TTAGTACCAC GTAGTGAAGC 900
CTTGTGGGCA GAGAAATATT GTCTCCCTTG TCGGAGGTAG AAATATCTGC AGGGTTTACA 960
AGCTAATTAC TTCTCGATTC CCTGGGAGTT CTAAGAATTT GCTTAGCAAC TGGCCTGACC 1020
AGTCTCCCCC AGCTGCCCCC CAACATGACT ACACTTACTG GTGGCGCTGA TGGAGCAGTT 1080
TTCGAACTAA ACAAGGATTA AGCATTTTGT GAAAATGGTG CCAGTCTTTT CCTCGATGGG 1140
ACCTGAGCCT GTAACCTAGT CCAACAAAAC GAGGGAGAAC AAGCCAAAAA AAACCTTTTT 1200
AAGAAACAAC ACAGGCAGTA GGAAATCATA CTGGTCAGGG CTTGTTTTCC TGGCGTGGGG 1260
CCTCATTCCA ACCTGTTGCA ATCAGCTCTA GAGTGTCTAT AGGGACACCC TGGTGCAGGG 1320
GCCCCGCGGA GGAAAGGAAC TTTTACATTT CTGTTTGACT GGGCTGCTTG CCAGGGACTA 1380
AGTTCAAAGT GCAGTTTCCA GTAATTTGCT GAGACTTCTC TGTGGGTTTG ATAGGCCAGG 1440
ACAGAAGCCT GCAAGCCGAA GTAATATTTC CTGATTTCTG TCATTCCTTA AGAAGAGAAG 1500
GAAGGTTGTT GAGGGACTAG GGATTGGAGA ATTTGTTGGC TCTGAGAGCA GATCGGACCC 1560
CCACTTCCCC CTGTCAACCC CAGCCCCTTC TCCTCAATCC CGTCTAGGGC CATTGGCAGC 1620
CTGGCACTAG ATGGAATCAC ACGGGCTCCC TCTCAGAGCA AACGTGAGGT ATGCATTCCA 1680
TGAGCCAGCG AAAGCCTGCA TTGATTTACT GCATGCTAGC ATTATTTGGA GCTATAAAGT 1740
TGTCGAGTAA TGGCAATATG TTCTTGTTTT CTCATATCTG TAGGATGAAA GTGAACATTT 1800
TTATAATCCT TCTCTCCTCA CCACATTTAG TTCCTGGTGT TAAACATGTG GGCTTGATTA 1860
AAGGGGAAAA AGAACTGCAA AAAGTTAGAT TTTTACATTC CTCTCTTACA ATGCCTCATT 1920
CCCTCAACCA TCCCCTTCCC AGAACACTGA TGGCAAGGCC CACATTCTTG TCATTTCCTC 1980
TTTGTCTCTC CCCTTCTCCC TGCCCTGTGT CTATCAGAGG ACTCGATGCA TAATAATTCA 2040
AAATGAATCT TTATTAAATG AAGGGGTAGG TAGTGGTGGA ATCTCACTTC AAAGAAGGGT 2100
TGGGTAGAAT GATATCGTTT CTATGTCTCG TAGAGGCTCA CAGGAATAGT GCTTTATTGA 2160
TTTTGATTAC AACTGCTTTT CTACAGCAAG 2190
|
