Tag | Content |
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EnhancerAtlas ID | HS060-33874 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr8:101475180-101475800 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MITF | MA0620.2 | chr8:101475245-101475263 | GTAAGTCATGTGACCAGA | + | 6.23 | MITF | MA0620.2 | chr8:101475245-101475263 | GTAAGTCATGTGACCAGA | - | 6.23 |
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| Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
SE_18537 | chr8:101474767-101476978 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19357 | chr8:101474800-101476994 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22743 | chr8:101474949-101476249 | CD8_primiary | SE_27991 | chr8:101475318-101476841 | Fetal_Intestine | SE_28830 | chr8:101475112-101476756 | Fetal_Intestine_Large | SE_32305 | chr8:101475087-101476367 | Gastric | SE_32533 | chr8:101474347-101477244 | GM12878 | SE_34085 | chr8:101475071-101477112 | HCC1954 | SE_47999 | chr8:101475715-101476254 | Pancreas | SE_62291 | chr8:101421434-101542088 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I100462 | chr8 | 101475138 | 101477142 |
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Enhancer Sequence | GGATTCAATA CTTCTTGCCT GAACTCCCAG AGTCGCCAGT CGACAAAGGC TTATTAAAAA 60 CCTCAGTAAG TCATGTGACC AGACAGAACT GATTCTAGCT CAGCCCACAG GAAGGGTAGC 120 CTTGCTCTCA GAAACCAAAT CTCTGGCAAG GCTGCCTTTA GGGTCAGATT CAGTGACATT 180 GGACTCCATG CTGGGGCAGA CCCAATCGGT GTGCCTAGGC CAAGATTCAG CAGGCCACAG 240 ATGCCTGGGG AATGAGCTTG ACCTCCTGGA GTCACTCCTT AAGAGAAGCA CCCAGCCTAT 300 ATCCCTGGGT TGTCCCACTT CCAACACAGC CCATATAATG CTGAAATTCA TATGCCATTT 360 ACTAACCTGT GCCAGATCAT CATATCACCC TCCCCTCTTT CTCTCAAGTG TGGTAGAAAT 420 GGCTAGTTGA CCCCTGAAAA GTCATGATCT CCTTGACTCC TTGATCTGTA TAGTATGAAC 480 TTGCTGTTGA GAAGCAGGTG ACTAACCAGG GACTCCATTT CCCAGCCTCT CAACCCACCC 540 CATGTCCTTC ACTCTGGCCA GTGAAATAAG AGCCTGAGAG ATGTGTCACT TTCTGGCTGA 600 GGTGGTTAAG TATCCAGTGT 620
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