| Tag | Content |
|---|
EnhancerAtlas ID | HS182-13266 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr2:225758960-225760080 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Rhox11 | MA0629.1 | chr2:225759026-225759043 | TTTCTTTACAGCATCAT | - | 6.08 | | SPI1 | MA0080.4 | chr2:225759221-225759235 | AGAAAGAGGAAGTC | + | 6.21 | | SPIC | MA0687.1 | chr2:225759221-225759235 | AGAAAGAGGAAGTC | + | 6.67 | | Sox6 | MA0515.1 | chr2:225758971-225758981 | CCATTGTTTT | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_11129 | chr2:225757515-225763655 | CD20 | | SE_18264 | chr2:225757474-225760548 | CD4p_CD25-_Il17-_PMAstim_Th |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 225759181 | 225759393 | | chr2 | 225759100 | 225759430 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I224893 | chr2 | 225758527 | 225760539 |
|
Enhancer Sequence | AGATGCTTTC TCCATTGTTT TAACAGAGGA AGAATACTGT GAATGTGAAA TCTCTAATTT 60
GCTTTCTTTC TTTACAGCAT CATGAATATA AGGAAAGATG AACAGTGTTT GGGGATACAG 120
CCACTGAAGA GTGTAATGGA CCTAAAGATG GTGGGAACAC ATTTAGTTAA AAGGATGGCT 180
AAATACGGCT GTCTCCATCC TCTCAACTTG AGATGCAGTC TCCCAACTTC CGAGTTGTAA 240
CCACTTCTCA GAACTATTTT CAGAAAGAGG AAGTCCTGAT GTTAAAAGAT GCTTTGCTTT 300
TCAGTTGTGC CTACAAAAAC TGTGTCATGA ACACCCAGAC ATTCTGAATG TAACAATTAC 360
TCATGAAAGC TTAGGGTGTG GTAAACCTTC CCAACATGAA GTTGCAAGAG CTTGTCTATC 420
AGCAGGGATT CAAGTCAAAA AGAATGCTCA AAGATCTGGT AAACGTTACT GTTCAGTGTT 480
TTGAAAAAAG ATTTGCAGTT TAGAAGGGAC ATACTTTTTT TCTCTTCACG GTAATGAAAC 540
CCCAAAATAA ATGGCCTCCT CCTGTCTTTT TCTTCGATTG CCACCCCTGC AGTCCCATTC 600
TCCATAGAGT AGCCCAAGAG TTCTTTCAAA GAGGTAAACC AGATCATGCC ACACCCCTGG 660
TTGAAATTTC CAAAGGCTTT TGTTGCAATG AAAGTAAAAT CCAAGCTCCT TTCCAGGGCA 720
CACAGGGTCC CTTGCCTAAG GTCCTTGGTT TCATCTTATT ACGCCCCTTT CATCCTTAAG 780
CTCTAGCCTT CCTGACTCAA GTGACCATAC TGGTTCCCAC CACTTCAGGG TCTTTGCCTT 840
GCTGCTTCTC CAGAATCCTT TCCCAAGATG CCTGTGTTGG CAGCTACTGC CGATTCATAT 900
CCAAGATCAA ATGTCACCTT CTTAAATCTA GTTCATAATC CCTCTTTCAA ATTCCGCATT 960
CGGAAATTGA GAGCAATGCT TCCAAGTATA CAAGTCTTGA AAAGGTGCTT CTGGGGCCAC 1020
AGGAAATATA GCAAAGTGGT TCCCAATTCT GTACCATGTG TCTATTAAAA ATTAGATCCA 1080
ATGTGTATCA TATCAGTGCT TCACTTGAGG AGAGTGTTAA 1120
|
