| Tag | Content |
|---|
EnhancerAtlas ID | HS042-31174 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr3:10233010-10234270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr3:10233584-10233598 | AAAGAATGAGTCAT | + | 6.6 | | RELA | MA0107.1 | chr3:10233977-10233987 | GGGAATTTCC | + | 6.02 | | RREB1 | MA0073.1 | chr3:10233730-10233750 | TGTGTGTGTGTGTGTTGTGT | - | 6.19 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_01374 | chr3:10232903-10233512 | Adrenal_Gland | | SE_01374 | chr3:10233588-10237950 | Adrenal_Gland | | SE_02168 | chr3:10232890-10237812 | Aorta | | SE_03544 | chr3:10232926-10234465 | Brain_Angular_Gyrus | | SE_05284 | chr3:10230421-10238972 | Brain_Cingulate_Gyrus | | SE_06271 | chr3:10230310-10239221 | Brain_Hippocampus_Middle | | SE_07281 | chr3:10230345-10238980 | Brain_Hippocampus_Middle_150 | | SE_08553 | chr3:10230394-10238941 | Brain_Inferior_Temporal_Lobe | | SE_10483 | chr3:10232905-10238935 | CD19_Primary | | SE_11117 | chr3:10230364-10244148 | CD20 | | SE_12182 | chr3:10233126-10238474 | CD3 | | SE_18222 | chr3:10230393-10242416 | CD4p_CD25-_CD45ROp_Memory | | SE_18887 | chr3:10230456-10239154 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19527 | chr3:10232850-10237954 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20302 | chr3:10232846-10239394 | CD56 | | SE_22972 | chr3:10232902-10238955 | CD8_primiary | | SE_27300 | chr3:10232887-10237905 | Esophagus | | SE_35045 | chr3:10230429-10236765 | HeLa | | SE_36305 | chr3:10230416-10237861 | HMEC | | SE_38379 | chr3:10230299-10236156 | HUVEC | | SE_46480 | chr3:10232852-10239588 | Osteoblasts | | SE_55870 | chr3:10232869-10239613 | u87 | | SE_58615 | chr3:10208482-10269048 | Ly1 | | SE_62498 | chr3:10211834-10316085 | Tonsil | | SE_64685 | chr3:10232624-10237158 | NHEK | | SE_67695 | chr3:10232869-10239613 | u87 |
|
| | 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 |
| GH03I010188 | chr3 | 10230458 | 10242599 |
|
Enhancer Sequence | CGTGACGCCC AGCCTAATTG CTAAGGAGGC AGGAGTATGA GACAGAGCAG ATGGTTATTT 60
GGTAAGTACT CTCTCAGCTA CAGGTTACCT CAGTTCCAGG GCGCTTACAG TAAGGTTCTG 120
CCTAACTGTG GCCTACAAGG CCCTGCATGG TCTACCTTTG CCCGGCTCTT CAACCTCACC 180
TCTACCACTT TCCCCCTCAG TCATTCCCCT CAGCCACTAC GGTCATCCTT CACTTGCGGG 240
GATATGCCAA GTGTTTGCTG CCTAAGGACC TTTGCACACG TGTTCCCTCT CCTTGGAATG 300
CTGTCTCTCC CCAGCTTCCC TACATTCTTC CATGCTAGTC CTTTTCATCC TCTGGGTGTC 360
TGCATATGTG GCCCCTTCTC ATGGCAGCTT TTCCTGGCCA GCCTATGGAA GTAGGTCCAT 420
CAGGCACCCC TCCCTCGAGT TTGTTTTCAG CATAGAGCAC CTCCCAGTTT ATAATTAGAT 480
GTCTTTTATT TAACTAGCTT AATGTCAGTA TTACGGCAGT TTTGATAAAG GATTCCCCAT 540
TCCCTAACAC AAAATGAATG AATGAATGAA TGAGAAAGAA TGAGTCATTT CAGCAGCAGG 600
TGGAGTACAA GTTCAGTGGA GAACCAGGGA TCGCACAATT AGGAAGGCAG GCTGTGCTCT 660
CAGGTTTGCC TCATTTCAGG TCTAGCTTGA GTTGGGAGTG TGTGTGTGTG TGTGTGTGTG 720
TGTGTGTGTG TGTGTTGTGT GTTGTGTGTG ACTGTGTATG GCCTGGAGGG CCAAACCCAG 780
GGATTAGGAG GGAAAGGAAA AGAGAGGGCG CGGAAAGCTG TGTTTGTCCC TGATAGAGCC 840
AGCTGGCACG AGGGTGCTTT AGTTATAGCT GAATCACTTT TGTTTGTTCT GGAAGGGATC 900
TATTCTGGCC ACATGAGTCA GCCTAAGAAC AAATTACTGT GTAGTTTGAC GGGCGTGAAG 960
GGTTGGGGGG AATTTCCAGA GTGTGCTCAC CCAGGAAAGA CCTTGTTGCC AGCTCTGAGT 1020
CCCCTCTGCT CCAACAGCTC CTGGATTTGC CACCGTGTGA AATGTTCTCA GGCAGCTAGT 1080
GTGACGGCCC AGGCCCCGTC AGCCAAAGGC CCAGCACCCA TAAACATCCT TTAGTCCTTT 1140
CTCCTGAAGG AACTGGGCCA TAAACAAGCA CATAATAAAT AAATCTGCAT TCTAGGCTTC 1200
GCTTTCTTCA GATATAAGAC AACTACCTTA TACTTGGTAG CAATTATCCC CCAGAGCTGT 1260
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