| Tag | Content |
|---|
EnhancerAtlas ID | HS183-03157 |
Organism | Homo sapiens |
Tissue/cell | T47D-MTVL |
Coordinate | chr3:169766460-169768680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Mafb | MA0117.2 | chr3:169767020-169767032 | TGTCAGCATTTT | - | 6.62 | | SP3 | MA0746.2 | chr3:169768345-169768358 | CACCACGCCCACC | + | 6.48 | | SP8 | MA0747.1 | chr3:169768346-169768358 | ACCACGCCCACC | + | 6.32 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28357 | chr3:169765752-169769108 | Fetal_Intestine | | SE_29014 | chr3:169760925-169769213 | 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 |
| GH03I170043 | chr3 | 169761100 | 169768921 |
|
Enhancer Sequence | TTATCACAAA AGCAACAGAT TTGTATTGTG GAAGATACAG GACAGTGTAA AAAGTAAACA 60
TGTACCTCTA TTCTCACCAA CCAGTTGCTG TTTGTGTCGC CGGGTTCTCC CCCTCCAGGA 120
CAAATGTCCT CTTCAGGCTT GCTCCATGCG TGGCCTGTCG GCTGGCAGCA TGGCATCACC 180
TGGGAGCTTG TTAGAAATGC AAAAGCTCAG GCCTGCCCCA GACATTGAAT CAGAATCTGT 240
CTTTTAACAA GATCTATATT CAAGTTTCGG AAGTCTTAGT CCCTGAGGCC ACCACCTTAC 300
CAGTCACGGT GGGCTGGCAT TAATTACCTC TGATCTGTGA ATATACGTAC ATTTTTCCTA 360
TTTCCCTGAT ACTGGGATGT ACCACTGTGT CTACCACTGG TTTGCACCCT CCTGTCTCCC 420
TTAACGTAAG ACCGTGTAAG GACAAGAGCA GGCTCCCCTC AGTAACACCG GTTCAGGGAT 480
CAGCAGGATC TCATCTCATC CCCCTATGAG AAGCCCTGCT ACACACAGCT TTATCTTGTA 540
TCTGTCATTT AACATTATAT TGTCAGCATT TTCCTGTTAT TTAGTTTTTC TCTCAAGTTT 600
ATCTTTCATG GCTGCAGGTG GTAATCCATC TTATGACTGT CTGATAATTC ATTTGACTCA 660
TTCCCTATTG TTAGACATTA AGTTGTTTTG ATTCTTTTGG GGACTGGGGA GGGTATACTG 720
TGGGCTATTA TAAGTATGCC AAAGTGAACT GCTTCCGCAG TAATTATTTC CCTCAACCCA 780
GATTATTTCC TTATGACAAG TTACCAGAGT GCAGACACTG GGTCAAAAGG CATGAACGTT 840
TTAAACCCTC CTTAAAATGC CGCAGGAGTA TACAAAGTGC CCTGACATGG TGCCCTCCCA 900
GACACTGGGT AGTGTGGTCT GTAGACAGAC TCCAGGGAGC AGGGTCATGC CTCATTCGCA 960
TCACGCCTCC AGGGCTGGTG TAGAGCCAAC TCTGAGGGTC ACTCTAAGGG GACCTGGGGG 1020
AATGGAAAGG AAGTGACGGA AGGATGGGCA AGCTGCCTGT GGTGGTGGTG CTCCTTTCCT 1080
CCTGGCCTGA GTCCTGAGTC ACAGTAGATG TCACTGACCA GGCAGCAGCC TTCCTCAGGG 1140
TGTGTCCACA AAGTTTAGCC TTTCCTCCCG GCACCCGTCT TCCAGTGGCT TGGGAGCTGG 1200
AGCAGGTGGT GGAGGCCTGA AATGACTACT TGGTGAGTCT GGAATGTGCC GGACCTGATT 1260
GCTGCCAAGC TTGTTTTTGC TTCACGAGTC TGAGACTGTT GGGTTCTCTA ATACTTTTTT 1320
CCTCTCACCA GCAGACCAGG AACCTGATAT TAAGTAAACT TTATTCTAAA AGGTACACTC 1380
AGACAATTCC TTTTTTTTTT TTTTGACACT GAGTTTCACT CTTGTTGACC AGGCTGGAGT 1440
GCAATGGTGC GTTCTCGGCT CACTGCAACC TCCACCTCCC AGGTTTAAGT GATTCTCCTG 1500
CCTCAGCCTC TCGAGTAGCT GGGATTACAG GTGCCTGCCA CCATGCCCGC CTAATTTACT 1560
TCTTCTTCTT TTTTTTTTTG TTGTTGTTGA GATGGAGTTT CGCTCTTGTT GCCCAGGCTG 1620
GAGTGCACTG GTGCGATCTC AGCTCACTGC AACCTCCACC TCCCAGGTTC AAGTGATTCT 1680
CCTGCCTTGG CCTCCCGGGT AGCTGGGATT ACAGGCACCT GCCACCATGC TTAGCTAATT 1740
TTTTTTTTTT TTTGAGACGG AGTTTTGCTC TTGTTGTCCA GGCTGGAGTA CAATGGTGCA 1800
ATCTGCTCAC CATAACCTCC ACCTGCCAGG TTCAAGTAAT TCTCCTGCCT CAGCCTCCCA 1860
AGCAGCTGGG ATTACAGGCA TGCACCACCA CGCCCACCTA ATTTTTTTGT TGGTCAGGCT 1920
GGTCTCTCTG CCAGTATACA ATCAGTTCCC ACCTGTAGCC CCAGATAGCC ATTGAACTTC 1980
TTTCTGTCTC TTGCCTTGTC TGGGAAATTT CAAATAAGAG GAATCTTGGG ATATGTAGTT 2040
TTATGTGTCA GGCATCTCTC ACTTAGCACA ACATTTTTGA GGTTCATCCA TGTTGCAGCA 2100
TGTATCAGTA GTTTGTTCCT TTGTATTGCT GAGTAGCATA CAGTTTTATA AATGTACTGC 2160
ATTTTATTTA TCCACTCACC AGTTGATGAA CATTTGAATT GTTCCCAGGG CTTGGCTATT 2220
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