| Tag | Content |
|---|
EnhancerAtlas ID | HS044-11033 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr6:11318280-11320120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr6:11318584-11318602 | AGAAGGAAGGAAGGAGGG | + | 7.97 | | EWSR1-FLI1 | MA0149.1 | chr6:11318580-11318598 | GAAAAGAAGGAAGGAAGG | + | 8.32 | | NFIL3 | MA0025.1 | chr6:11318721-11318732 | ATGTTACATAA | - | 6.32 | | ZNF263 | MA0528.1 | chr6:11318589-11318610 | GAAGGAAGGAGGGGTGAGAGG | + | 6.25 | | ZNF263 | MA0528.1 | chr6:11318593-11318614 | GAAGGAGGGGTGAGAGGAAGG | + | 7.93 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_09363 | chr6:11317329-11320333 | CD14 | | SE_11222 | chr6:11314264-11321496 | CD20 | | SE_38711 | chr6:11314939-11320263 | HUVEC |
|
| | 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 |
| GH06I011315 | chr6 | 11315572 | 11319929 |
|
Enhancer Sequence | TTGGACTTAA ATGGAGATAT CAGATCTTCC TGGGTCTCAA ACCTGCTGGC CTTTGTGCTA 60
GAGCTATGTG ATCCGCTCTC CTGGGTTCCA GAGCCTCAGA CGCAGACAGG AACCACACCA 120
TCAGCTCTCT TGGGTCCCCA GTTTGCCAAC TCATTCTGCA GATCTTGGGA CCTGCCTGCC 180
TCCATGATCA CATGAGCCAA GTTCTTACAA GAAATCACTT TCTAAATATA TATGTGTATC 240
TTATTGGTTC TGAGAACCCT GAGTAATGCA GCACAAAATG GAAAAGAAAA GAGAAAAATA 300
GAAAAGAAGG AAGGAAGGAG GGGTGAGAGG AAGGTGTGGA GCGGGGGATG AGAAACACAG 360
CCTCTGTGCT TTGCAAGTGT GGGGAGACGG CGGGTCACTG CATCATTGTC TGTGATCGCT 420
GACGGCGTTG ATGACTCACT CATGTTACAT AATTAGAATT CACCTTCAGA CTTTGCTGTC 480
TTACCATTTC GTCTCATAGA AACAAGGCTT CCTAGCTTGG CTTGTTTTCT TGTTACTCAG 540
GGGCTGTTGC TAGCATAAGG TCATACTTAG AAAGCTGAAC CCTCAATAAG ATTACTCAGA 600
GACTTGGCAG CTTTTTCCCT GGCCATTTTG TCTTTAAGTT AAAAAAAAAC AACAGAAAAC 660
AGCTCACTCT TCTAAAATGA CATTACACAT CACTTTGAAA TATGTCCTGT AGGCCAGCCC 720
TGAAATGTAT GGTCTTTCTG GACATTCATT GGAGAGAAGC TCTGTTTTTA AAAATGTAAA 780
AAAAAAAAAT TGTTTTACTC TAAAAGAGCG TCTCTGATAA CCCAGTTTTT AGGAAACTAT 840
TGGCTGAAAA GAAACAACAG GAGAGGTGAG AATTTGTCCA GTTTATACCT AATTCATTTC 900
TGCCATTATC CCATTCTGGG ATAACTTCAG AAACCACGAG GGCCATTTAA CCAAGAGATT 960
TATTGGGCCT TAGAGTTCAT TATGTTTCTG CCTTGTTTTT ATAATGCTTT TGTTATAATA 1020
TTAAAGTGAC AAAGATAAAC AACTTTATTT GTGGTTGTGC AGATGCCATG TGGAATATCT 1080
GCTCGGCTTG AAAAGATTCC CCTGGCTCTT CTGCCCACTC AGAACAGCGG GACCCACATT 1140
TCAGCTTGGA CAACATGACC AAGCTCTGCT GTTCACAGCT GCCTGGCCCA GGCTGGGTGC 1200
CTGGCCCCAA GTTCAGGGCC AACGCCCTTT TCTGGGAATG GGGAATCAAA GCAGAAAAGC 1260
ATCCTGTGCA CTCACACTCT CACACACCCA CACACTCACA TGCACACTCA CATGCACACT 1320
AACATACACA CAAGTCTCAC ACTCACACAC ACTCATGCAC CCTCACATAC AGTCACACAT 1380
GCACACTCAC ACACTAACAT GTACACACAC ACTGGTACAC ACTCACACTA ACAAGCAAAT 1440
AATCACACAC TCATGCACAC ACACACTAAC ATGCACACTC ACACTAACAT GCGGACACAC 1500
ACTAACATGC GGACACACAC ACTAATATGC ACTCACACTA ACGCACACAC TAACCATGCA 1560
CACTCACACT CACACACACA CACACTAACA TGCACACTCA CACATGCCAC ACACTAACAT 1620
GCACACATAC ACAAACATGG ACACTCACAC AAACATGCAC ACACAAACAT GCACACTCAC 1680
ACACTAACAT GCACACACAC ACTAACATGC ACACTAACAT GCACACTCAC GCACACTAAC 1740
ATGCACACTC ACACACTGGT GCACACTTGC ACTAACAAGC AAATACACTC ACGCACTCAT 1800
GCACACTCAC ACACTCATAC ACACTAACAT GCACACATGC 1840
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