| Tag | Content |
|---|
EnhancerAtlas ID | HS182-20507 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:8939250-8940420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr8:8939647-8939660 | TTCTAGAACCTTC | + | 7.12 | | SOX10 | MA0442.2 | chr8:8939739-8939750 | TTCTTTGTTTT | - | 6.62 | | TCF7L2 | MA0523.1 | chr8:8940022-8940036 | TTCCTTTGAAGTCC | - | 6.11 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27764 | chr8:8931616-8940631 | Fetal_Intestine | | SE_28660 | chr8:8931504-8940665 | Fetal_Intestine_Large | | SE_38116 | chr8:8937421-8942637 | HUVEC | | SE_56603 | chr8:8938338-8941106 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 8939736 | 8940088 | | chr8 | 8939402 | 8940318 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I009073 | chr8 | 8931488 | 8940483 |
|
Enhancer Sequence | GGAGTTTAAT AGGCAAGAAA GAAGGGGGAA GAAAGAAAGA AGCTCCCCTG TACAGAGACA 60
AAGGGAGGGG TGCTCCAAAG CCAAGAGAGG GAACCCCCAC AACTCCCATT TCTTATGAAA 120
AATAAGCAAT TTAATTATTC TATGTCTAGA CTTCTCATTA GCCTGCACTG GAAGACCAAA 180
TAAACCCATT AATATTGTTT TTCTGAGCAA AAGTTGTTCT CTCTGTATGA AGAATTCTGC 240
CTTCATCTTA GTCCATCTGG ACCCTGCAGC CAACTTTTAA AGTCACTGTG TCCCCCCACC 300
CCATTAGAAC TCTTAATATT TGTTTAACCT CAGAGTAGAA TGGAAAGCAT GAATGGCAGA 360
TATTTCTTAC GACTCCAGGA AGTGAAGTTT AGTCTCTTTC TAGAACCTTC CATCAGGTGA 420
GGTCCACTAT GAGCCTGGTT TAGAGGGGAA GGAGAATGGA GACCCTCACA ATGTCCTAAG 480
ACTCTTGTTT TCTTTGTTTT TCTTGTTTTC CTCTTACTCC TTTTACCAGA ACTTCTGGCA 540
AGTAACATGT TGACTCATGG TGTTTTATCA CTTCCTTCCT CTGGCTCACG TCCAGTAGAC 600
ATGCTAATGA GTTGCCAAGT CACCAGTAGG CAGGAAAAGA CAGAAGGGCT TCTCTGCCAT 660
GGAAACCTGA TCATCTGGTG TTAATATTCT GAAAATGACA TTCACAAAAT GAGAGTTAAG 720
CTGGATGAGA AGGTATCTCC TGCTTTCTGG CATGAAATCA TTCTTCCTTT GTTTCCTTTG 780
AAGTCCATAT CTGTGTAAAA GATGCAACAG CAGGAATGAT CTGTACTTCT TGGGGGTCTT 840
AATCTCTGCT GTGTTGAAAG GATATTGAAA GAAATGGATG AGGACCTACA TCTGGGCTCC 900
TCATCTTAGA AAGTAGGCAC CTGCTTGGGA ACACTTAGGC AAATGGATTC TCTCCTTCCC 960
CATTTCCCTT CAGGGGCCAG AAGGTCGGAC AGAAAGTCCA CCCTTGAACC TATCTAACGT 1020
CTAGGAGAAA GTCTTTCTAG AAACATAGAG AAAGTGAATG ATGAGATGCC CGAAGAGTCA 1080
TAATAGCAAG AGTCCGGTCT AGTCAGTTCA GGGTGAACTA AGACATGGAA TGCATTGGAG 1140
AAAAGTGGGG ATGATGGAAT ATCCTAAATT 1170
|
