| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00600 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:29503100-29504360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:29504012-29504027 | TGAACTTATGACCTT | - | 6.26 | | RARA | MA0729.1 | chr1:29504009-29504027 | TCTTGAACTTATGACCTT | - | 7.17 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_00764 | chr1:29501997-29509898 | Adipose_Nuclei | | SE_28354 | chr1:29503699-29504554 | Fetal_Intestine | | SE_29089 | chr1:29502773-29509804 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 29503111 | 29503245 | | chr1 | 29503419 | 29504100 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I029176 | chr1 | 29503017 | 29503805 | | GH01I029177 | chr1 | 29503912 | 29504410 |
|
Enhancer Sequence | ATTCAGGAGT CAAAAGAGAA AAATCCCTGT GTAGGTGCTG GGGTTGGCAG TAATTCTTCT 60
CAGTATCTAA GGCTTAATAA TGCCCTCCAG TGAGCAGTGA CATACACAAC AACGACCTGC 120
CTCACTCGAA GAGTCTTGAA CTCCACATTA AAAAAATTAT GGTGCATTAA ACAAGGGCGA 180
AAACAAAAAT TTTCTGGTAA TAATTAGATA GCATGACTAA ACAGACCACA ACATCCCCTG 240
AAAATTCAGG CTATTCATGA TTTCACTGTT CCATGAAACG CAGGTTCTGA AGTTTAAATC 300
CAAGTTTCCC TTGAGAGTTT TAATTCATGA CTTGAACTAA AAAATAAAAC TATAAATTTC 360
AATGATCTGG GGGTTTATCC TTCTAGCTAC TAGACAGGCA AAATAATCTT AATATGTGGT 420
AAGTTTTACT CATTAACTAA AATATGGAAA AGCTAAGATA TAAAGATCTG ACTAAAACCA 480
CAAGATTTTA TGACAAAAGG GCAACTAGTG TACTCAAAAT TCTTTCACAC TTTACATGAA 540
ATGGCTTATT ATAAAAAATA AAATCTATAT ACAATCAAAG CCAACAAAAG TTACCACAGA 600
GCTGAAAGGG TATAAACAAG TGCTGCTAAT ATTGTTGCTT CCTTGACGTG CATCTAGGAT 660
TCCTGCCCCT CCCTTCCCTA CAGTAACTCT TTTTGTTTTT TTTTTTTTTT GAGACGAAGT 720
TTTGCTCTTG TTGCCCAGGC TGGAGTGCAA TGGCAGGATC TCGGCTCACC GCAACCTATG 780
CCTCTGAGGT TCAAGTGATT CTCTTGCCTC AGCCTCCCGA GTAGCCAGGA TTACAGGCAT 840
GTGCCACGAC GCCCGGCTAA CTTTGTATTT TTAGTAGAGA CAGGGGTTTC TCCATGTTGG 900
TCAGGCTGGT CTTGAACTTA TGACCTTGGG TGATCTGCCT GCCTTGGCCT CTCAAAGTGC 960
CGGGGTTACA GGTGTGAGCC ACCGTGCCAG GCCCTTGCAG TGACTCTTGA AGTTTATGGG 1020
GCGGGTAGAA AAGTAGGAGA CCTTAATGGG AAATGGAATG GTCTATATGA TCCTGGGAGA 1080
TCTTCGTTGT ATTTGTGGTC CCAAACCATC TTTCAAAAAG TTCTCTAGAA CAGTGGCAAT 1140
CTACATTAGC GATGCCTGGT GTAATAAAAC GGTAGGCAAT GAACTCTTGC TTACACACCT 1200
CTTCTCCAAA CCCTCTCAGG GTCCATAGAA TCCTTTCCTG AACACTAAAT CTCCTTTGAA 1260
|
