| Tag | Content |
|---|
EnhancerAtlas ID | HS136-04625 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr12:52438520-52440190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr12:52439627-52439642 | TGACCTTTCACCCCT | - | 7.08 | | Nr2f6 | MA0677.1 | chr12:52439627-52439641 | TGACCTTTCACCCC | - | 6.42 | | Rxra | MA0512.2 | chr12:52439627-52439641 | TGACCTTTCACCCC | - | 6.91 | | ZNF263 | MA0528.1 | chr12:52438757-52438778 | GAGGGAGGGAGGGAGGGGTAG | + | 6.03 | | ZNF263 | MA0528.1 | chr12:52438761-52438782 | GAGGGAGGGAGGGGTAGAGAA | + | 6.82 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_01015 | chr12:52435153-52439880 | Adrenal_Gland | | SE_01838 | chr12:52434996-52440307 | Aorta | | SE_04021 | chr12:52437429-52438834 | Brain_Anterior_Caudate | | SE_05966 | chr12:52434736-52440443 | Brain_Hippocampus_Middle | | SE_07218 | chr12:52438991-52440241 | Brain_Hippocampus_Middle_150 | | SE_07944 | chr12:52436304-52438690 | Brain_Inferior_Temporal_Lobe | | SE_23310 | chr12:52438855-52440455 | Colon_Crypt_1 | | SE_23835 | chr12:52438975-52440317 | Colon_Crypt_2 | | SE_24905 | chr12:52438752-52440476 | Colon_Crypt_3 | | SE_26342 | chr12:52437368-52440192 | Duodenum_Smooth_Muscle | | SE_27026 | chr12:52436630-52440170 | Esophagus | | SE_30252 | chr12:52436202-52440199 | Fetal_Muscle | | SE_34732 | chr12:52438786-52441666 | HeLa | | SE_38567 | chr12:52437329-52440581 | HUVEC | | SE_40781 | chr12:52432004-52441428 | Left_Ventricle | | SE_44280 | chr12:52436246-52440436 | NHDF-Ad | | SE_45503 | chr12:52436980-52439048 | NHLF | | SE_46044 | chr12:52436454-52439748 | Osteoblasts | | SE_46664 | chr12:52438381-52439987 | Ovary | | SE_48081 | chr12:52434946-52451493 | Psoas_Muscle | | SE_48629 | chr12:52432026-52440456 | Right_Atrium | | SE_49724 | chr12:52436227-52438951 | Right_Ventricle | | SE_49724 | chr12:52438960-52439972 | Right_Ventricle | | SE_50349 | chr12:52435776-52440428 | Sigmoid_Colon | | SE_51135 | chr12:52434177-52441905 | Skeletal_Muscle | | SE_52700 | chr12:52436525-52440371 | Small_Intestine | | SE_53734 | chr12:52436521-52440520 | Spleen | | SE_54908 | chr12:52434951-52439255 | Stomach_Smooth_Muscle |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 52438699 | 52439014 | | chr12 | 52439738 | 52439919 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052041 | chr12 | 52434810 | 52441615 |
|
Enhancer Sequence | AATTTGGTGG GTGCTGATGT TCTGCAAGGT GGTGGGAGAC CCTCCAAGGC GAGAGGAGAA 60
GAGAGCTGGC CAGGAGCTGA AGAGACTGAG AGGGAAACTG AGGGAGGTTC AAGGCGTGGG 120
GCAACCTTTC CCAAAGGAAC TCCGTGATCT TGTCTGTGTT TTCCAGCCCC GTCTGGTGGT 180
TCTTCCTGAA GTCTGATCTT ATTCTTTTAT GCTGTATGTT AATTTCTTCT GGCCTGAGAG 240
GGAGGGAGGG AGGGGTAGAG AAATCACTGG ACTGAAGATA GCCTCTGTGG CCATAGCCTG 300
ACCTCCTTAA TTAACTAGCT CTCTCCAGAG TATTAATTGA CCACTCGCTG CATACACAGT 360
CTAGAATTCT CCCAGTGCTG GGTAGAGCCA CATCTCTGGG CACACTCTCT TTTCCTCTCA 420
CTCAGCCCAG GAGTGGGAGA AGTAGAGATG GGGTTACTGT TTGTCTGTAG TTCCTGGAGC 480
AGGAGGGCTG CCGGCTCCCC CGTCCAGCTG AGGACCCTGC TATCTCCTGC CCCTGCCACC 540
CTCCCTGCCA GCCCCAGGAT TCTGCTGCAG GCTGCTGTGG TTGTCCCGTT GCAGACATGA 600
GTTCCACAGG GCCGAGTGTG GGACTTGAGT ATGCATGGAT TTTGGTATAT GTCGGGGTCC 660
TGGAACCCAT CCCCCTGTAG CACTTCCCTG TGCCCTGGAG GTACTGCCTG CCTCCCGACT 720
TCCACCCTCA CTTGCCATTA CAGGTTTCCC ATGACAGTGG GGGAGCCCAG GCCCCAGGCA 780
GTGCTACATT TGGATGTGGA GCCTCTCCTT TCCATTGTGA ACTGAATTCT ACCAGCACTG 840
GGCCTGGTGA TGTCTGCATT AGGCAGATGA GGAAGCAGTC TTGGAGAGGA CAAGGGACTG 900
GCCTCAGGTC ACACATCAGG CTTGCTAGCT CCTGGACAAA GATGCCTCTG ATAGCTCTTC 960
CATATTTCGC CCCTGCTGAG AGCTGAGGGG AGGAGTGCGG CCACTAGCTG ACCTGCCTGG 1020
GTCCCTGGGA GGCTGGTTTT GGGGAGGTAG TGATACATGT GCTCATGGTA GGGCTTGGGC 1080
AAGGGCCAGG AGAGCAGAGC CTGGGCCTGA CCTTTCACCC CTGGTTCCCA GAGCTGCCCA 1140
CGGGAAGCCC CCAGGGCAGT AGGCAGTGCT TCCCTGCCCA CAGTGCAAAT CCCCCTGCCT 1200
ACTGCCAAAG CAGGAAGAGG AAGTGGCCGG GTCAGGGCTG GCAATAGGCC CTGGGGCCGA 1260
GGAGGGGAAG CTCCCAGGGC CACTTCTGAG CTGGAGAAGG CAAAGCTCAC TCCTTCTGCC 1320
CACCCCAGGG GAAGGGTGTG GAGGCCCATG GGTGGGGACA GTCTCAGTGA AAGTAGGGCA 1380
AGTTCCTGAC CTCTACTCAG TAGGGGTGGG GCCCAGCCCA AGGTGGAGGG GCAGCGTGGG 1440
AAAAGGGCTG TGTAATTCCA CTTCCTTCAT CCCCTGTTTA CCCATCTCCA CCCCTACCCT 1500
CTGGGCTGGG GAATGGTGGT GGACATTGGC TGCTCACTTG GGGCCTGCCC TGGGCTACTT 1560
ACTACTGAGG ATGCACAAAG GATCTTCCCA CCACGGACTA GGAGACAGTG CCCTTGTCCT 1620
CATGTTGTTC ACATACTGGT CGGTGAGGGA TGGGTCTGAG TACATGATAA 1670
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