| Tag | Content |
|---|
EnhancerAtlas ID | HS098-40196 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:138581500-138582660 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr3:138582383-138582394 | GGTGACTCATG | + | 6.62 | | HNF4G | MA0484.1 | chr3:138582059-138582074 | AATGTCCAAAGTCCA | + | 6.09 | | JUND | MA0491.1 | chr3:138582383-138582394 | GGTGACTCATG | + | 6.02 | | SPI1 | MA0080.4 | chr3:138581620-138581634 | GGAAAGAGGAAGTG | + | 6.1 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_28317 | chr3:138579409-138583350 | Fetal_Intestine | | SE_28944 | chr3:138579488-138583347 | Fetal_Intestine_Large | | SE_35774 | chr3:138580315-138583349 | HepG2 | | SE_40235 | chr3:138580999-138583176 | K562 |
|
| | 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 |
| GH03I138860 | chr3 | 138579619 | 138583421 |
|
Enhancer Sequence | AAAGTGAGAA CTCAGGGTCA GGGCAGAACC AGGAAGAGAG CAGTGAGATA TCCTGCTACC 60
TAATCCAATT CTCCTTTTTG TGCATTTAGC ACCCTCCCCT CCGCCTGCAT AACAATGGAA 120
GGAAAGAGGA AGTGGGAAAA AAGAAAGTCA TGTAATTGAG TTAGAAGAGG TAATGACCAA 180
GACCCTGGAG CAGAGGGAAA GCGGGTTACA AAAGGTGGGT TAAAGAAATC ACAAGAGTAT 240
GAAGAGCTGG GAAATTACTA ACAAATATTT GCTTGTGTGG GAAAGCAAAA AAGTAAAAAC 300
TTCAGTGCTG AATTGGGGCG CTGAGCCACC AGGGAAATTT GAGATTGGCA TCAAGGACCG 360
TGTTGAAGCA GGGTGGGCGG AGAAGGAGGG AAAACTACCA GCCAGCTGAG ATTTTGCAGC 420
TAGGCTGTGG CCTGATACCG AGTATCGATG CCGCAAGGGA GGGATGAGTC AGTCCTAGCA 480
CGTCCAAGTT TAGAATAATA GACTGTTTGC CACTGGGAAG GCAAACACCT TTCCTGTGAG 540
AGGGCTTGCT GACAGTTCCA ATGTCCAAAG TCCAATGCCG ACCCAGAAAA CTGAGGAGGC 600
CCTGGCCCCT GCAGGAAGGG CTCATTTACA TGGAGACTGA GTAAAGTGCT GTCTTAAACC 660
CTCCTTCCTT CCCCCACTGG GAGGTTTCAG CCAGATATGC CACCCTTTGT AGGATTTCAT 720
AGGGTTGTCT AAAGCCAGGG TTGGCACAGA GCAGAAGCCA CAGGGCTAAG TACCAGATTA 780
TAATTGTCAA TGTCACACCT TACTGCAGAA GCCAGGGAAG GGAGCTAGGA AACTGAAGAG 840
CTTTCTTGGT TATGGGCGGG GCTGTAAATG CAGAGTGTGC CCTGGTGACT CATGGGAGAC 900
AGTGAGAAAC ACTGTGGGGA TCTGGTCAAC CGGGTACTGA TTCCTTTGAG GAAGGTATAC 960
TCCACATGCC AACCTGATAC TCATGGCTAG TGAAGAGATG GCAGGATTGG GTTGCATCAG 1020
CCAGCCTAAC TCGACTTGGA AACACAGAAA ATAACCCAGA GCAGGTCTCA AGCACTGTGT 1080
AACTTTATTA GTTCATAGTG GCTGAACAGC CATGTTTAGG GCCTCTCAGA AGAAAGAGTT 1140
TCATCTTTGG GAAGAAATTT 1160
|
