| Tag | Content |
|---|
EnhancerAtlas ID | HS044-04378 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr14:78046870-78047920 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr14:78047432-78047453 | AACAAGAAAACGAAACTACAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09589 | chr14:78046812-78048168 | CD14 | | SE_13603 | chr14:78047176-78048331 | CD34_Primary_RO01536 | | SE_14261 | chr14:78046872-78047776 | CD34_Primary_RO01549 | | SE_46228 | chr14:78044914-78048478 | Osteoblasts |
|
| | 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 |
| GH14I077580 | chr14 | 78046788 | 78049542 |
|
Enhancer Sequence | CCTTTAGAAA GGAATTTTTT AAAAAAGAAA AAAAAAAAAA AAAAAAGAGG CCAGGTACAA 60
TGGTTCATGC CTGTAACCCC AACACTTCGG GAAGCTAAGG TGGAAGGATC GCTTGTGGCC 120
AGGAATCTGA AGTGACAGTA AGCTATGACT ACACCACTGC ACTCCAGTCT GTGCAACAGA 180
GCGAGAACCT GTCTCAAAAA GAAAAGAAGG CAGGACACAG TGGTTCATGC CTGTAGTCCC 240
AACACTTGGG AGGCTAAGGC GGGAAGATCA CTTGAGCCCA GGAGTTCAAG ACCAGCCTGG 300
GCAACATAGT GGGACTCTGT CTCTACAAAT AAATTTTTAA AAAGAAAGAA AAGAAAATAC 360
ATTCCCAAAA TGAATTCCTA TGCTCAGGAA CTTAACCCTT CCTCTGAGAG ATTAAGTTGT 420
ACTAAAACTT AAGTCTGTAA AAAATCAAGT CACAGCGGAG CAGAAATGCT ATGCCTGGTG 480
TGGTATGACC ACTACTCAGA ACACATGTGA CCAGACCATA TGAGATCTAC TTAAACTCTT 540
GAATGTAAAG GGTAAACCAA ACAACAAGAA AACGAAACTA CAGTTTTTAC TGTATCAGCC 600
AACTACTGAG TTTATAACCA TTAGATCTGG GCTTGGTGCC AATATAAATT AAGCTGTTAA 660
CTAAATCAGT CAAAAACATT GAAAAAGCTT AAGCCTTATT CTGTAAAAGA TTTTCATTGC 720
TAAAGAAGGC TGCATACAAC TCTAAAATTA ACAACTTTCT ATGACACCGG ACTCTCAAGT 780
GCCTATTGAA TGAGCCTCCC AGTAGATAAA TCTTATAAAT AAGGCTGAGC AAAGTCAGAA 840
GCTACTCTAA GAATTTGCAG TACCTGATAC CATCTCTCTT TTTTTTTTTT TTTTTTTTTT 900
GAGGCAGAGT TTCACTCTTG TTGCCCAGGC TGGAGTGTAA TGGTGTGATC TCGCCTCACT 960
GCAACCTCTG CCTCCCAGGT TCAAGCGACT CTCCTGCCTC AGCCTCCCAA GTAGCTGGGA 1020
TTACAGGACT CTGCCACCAT GCCCAGCTAA 1050
|
