| Tag | Content |
|---|
EnhancerAtlas ID | HS056-09006 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr2:128161860-128162980 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr2:128162849-128162870 | GAAGGAAGGGGAGAATGGAAG | + | 6.17 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_09644 | chr2:128161566-128163674 | CD14 | | SE_23461 | chr2:128162089-128163742 | Colon_Crypt_1 | | SE_24894 | chr2:128162155-128163022 | Colon_Crypt_3 | | SE_28345 | chr2:128161917-128164000 | Fetal_Intestine | | SE_29146 | chr2:128161921-128164000 | Fetal_Intestine_Large | | SE_50833 | chr2:128161990-128163780 | Sigmoid_Colon | | SE_52838 | chr2:128161824-128163771 | Small_Intestine |
|
| | 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 |
| GH02I127404 | chr2 | 128161977 | 128163977 |
|
Enhancer Sequence | AAAGCATCTC CCCCACAGGA CATTTATTAA TTACAAAGGG AAAATAGCAA CTTTCCAGTG 60
GAGAAACTTC AGAGACACCA CTTTAACCAA GTGATCCAAG CTACCATGAC CAGTAATGAG 120
ACATATTATC ACCCCGCCCT TGACAGTGTC CTGAGAGGCG CACAGCATCA CTTCTTTGGC 180
ATTTGTGCCA AAAATGCATA TCCTCAATCT AATACTGAGA AAACATCAGA CAAATCCAAA 240
GTGAGAAATG TCCTATAAAA TAGCTGGCCA GTGTCACAGC GACAAGGAAA GACGGGGGAA 300
CTGCCCCACA TGGGAGGAGA CAAGTGCCAT GTTGGATTCT GAATGGGATC CTGGACTGGA 360
AACAGGACAT CAGTGGGACC CAGGGGGCAA TGGCAGGGAG AGGTGCGGGA CCCAGCTGGG 420
ACATCTGCTT TCGGGACTCT GCTTTCGTCC CCAGCGGCAA TCAAAGATGC ACCCCTCTGC 480
CAACCACAGC AGTCTGTGAT TAGATGTAAT GGAGGCTTCA GGATCAGAAT GATCCAGCAA 540
CCTGGCTCTG TTTCTCTCTG ATTTCCTTAA TCACATCCTC TTCTGGGGCT GTCTTTGTTG 600
TCAGGCTGCC TCCTTCCTGA TAGCCAAATG GTTCTTGAAG TTTCAGTTCC CATATCTGCT 660
TGCCACTCTG GAGGAGAATG AGGGCTCTTC TGGTAGTTCT TTCCTTAAAG AACAGGAGCA 720
CGTTTCTTCC CCAGAAGTCT CCAAACTTAT CCTCATATTT CACTGGGCTG AATTTGATTA 780
CAAACCCATT CCTGAAGTAA ACCTTGGGCC AGGAAATGCC ATGCACAAGT TGGCAAATGC 840
AATGGGATCA CTCTCTGAAA AATCAGCTTC CCAACCCCCA CTCAGGAGCT GCAGGCAAGG 900
GGCTGAGCAT GGGTCAGCTT TCCCTGAAGC ATGTGTAGAC AGGCAGATAC CTGAACAAAA 960
CTGGGGTGCT AAAACTGGGG TGCTATTAGG AAGGAAGGGG AGAATGGAAG CTGGGTAGGC 1020
AACAGTGTCC ACAACTCCAA GCAGTGTTCT CTTCTGTAAT AATTGCCTTT CCTGGTGGAG 1080
TTTCCTGTGG ACCAGGAGGA TGCCTGCAGC AGGCACGGAC 1120
|
