| Tag | Content |
|---|
EnhancerAtlas ID | HS098-39992 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:129317770-129319170 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr3:129318643-129318664 | TTCCCCACCACGGAGAGCTCA | + | 6.15 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_00112 | chr3:129305417-129325570 | Adipose_Nuclei | | SE_00978 | chr3:129313612-129319284 | Adrenal_Gland | | SE_01893 | chr3:129313676-129319163 | Aorta | | SE_04322 | chr3:129310378-129319241 | Brain_Anterior_Caudate | | SE_05345 | chr3:129310701-129325499 | Brain_Cingulate_Gyrus | | SE_05951 | chr3:129308023-129325521 | Brain_Hippocampus_Middle | | SE_07365 | chr3:129310382-129319614 | Brain_Hippocampus_Middle_150 | | SE_08750 | chr3:129311577-129324158 | Brain_Inferior_Temporal_Lobe | | SE_09767 | chr3:129314862-129320344 | CD14 | | SE_25754 | chr3:129308309-129320001 | DND41 | | SE_26494 | chr3:129314001-129319380 | Duodenum_Smooth_Muscle | | SE_27065 | chr3:129313676-129319366 | Esophagus | | SE_29874 | chr3:129310485-129319205 | Fetal_Muscle | | SE_31569 | chr3:129313699-129319812 | Gastric | | SE_37506 | chr3:129314013-129319542 | HSMMtube | | SE_37994 | chr3:129310132-129325566 | HUVEC | | SE_40701 | chr3:129308079-129325658 | Left_Ventricle | | SE_42115 | chr3:129307923-129325621 | Lung | | SE_46476 | chr3:129310313-129319510 | Osteoblasts | | SE_47266 | chr3:129310010-129324076 | Panc1 | | SE_48609 | chr3:129310376-129325641 | Right_Atrium | | SE_50249 | chr3:129311586-129319771 | Sigmoid_Colon | | SE_51354 | chr3:129310040-129325518 | Skeletal_Muscle | | SE_52687 | chr3:129313665-129319687 | Small_Intestine | | SE_53375 | chr3:129310325-129320850 | Spleen | | SE_62855 | chr3:129293187-129347490 | Tonsil | | SE_65523 | chr3:129313701-129318953 | Pancreatic_islets | | SE_68869 | chr3:129314894-129320007 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 129318000 | 129319000 | | chr3 | 129318465 | 129318690 |
|
Enhancer Sequence | AGATATGTAA AGTGCTCTGC AAAGGGCTAA CACAGAGAAA GTTCTCAAGC AACAACCACA 60
GTAATTATGA CATGATGGGG CAGTTCTGGT GTCAGAGGGA AGGCTTCCTT GCCACTCCAT 120
GGGCCAACTC CAGGGTCGGA GAACGGAGGC CCAGGTAGGG GAAGGCACCA CTCTCTCCCG 180
GGGCTCCTGC CCTCCCGCTC CTGTCCCAGT ACACGCCACG CGTCTTTGTT CACGGCAGCA 240
ACCAGGACAT GGAACCCAGC TGGTTTCCTT AATCTCCATG GAGACCGGGA GTCACAGGCG 300
GGTGAATCGG ACTTTGCAGA GGGCGTTTCT GCCGGGCCCG ATGCGCGTGG CCCTTGCTGA 360
ATGCCGCCAG GCCACTCCAG TCTTCCCTGC GCTCAGCCCA CTTTATAGAT GGGAAAATGG 420
AGGCTCCAAG AACGGATGGG ACTTTCCACA GCTAGGAAGG GGCAGAGGCA GGATTTGAAT 480
CTGGGAAGTT GGCCCCAGGG TCCTGCACTC ACCTAGCGAT GTGCGCCTGC CTGGCTGTGG 540
AAGGCCTCAC TGTGGGCGTA TCCAGGGCGC TGACAGATCC CCCACTCACC CTCCTGGGTG 600
GACCATCATT CACACTGACC ATTGAACCCA CATCTCTCAT TTGCACACCC AAAGGGCCAT 660
GGGCTCACTC CTTCCAGAGG CTGATGATCG CATTTTCAGA CAAATGCAAC TAGAAGTTCC 720
TTGCCTCCCC TGACTTCCTC AGGAAGCTGG GTCAGCCCCC ATCCCCCAGC ATGTGGCCTG 780
GCCTCTGCAG ATGCCCCAGC CCGCCTGAGT CACTGCTATC ACAATGGGCC CTGCCTGAAT 840
CTCTATGGCC CAGCCAGAGG GGGAACTGCA GAATTCCCCA CCACGGAGAG CTCACAGCTC 900
ACCAGCCACC AGGAAGAGGA CTCCTGCTTC TATCTGCGGA TCCAGACCCT CACTCCCCAG 960
CTGTGTGAGC CAGGGCAAGT CACTTCCCCT CTCTTGGCCT CAGTTTCCCC TTCTGTAAGC 1020
TGGGGATGAT GATGACGCAC TGTCTGCCTG ACCAGGGGAG GGGCAGCCAT GAGGTCAACC 1080
ATGTAGGTGC TTATAAAAGG CCTGCAGAGC GCGAGCTCGG CGACGGTTTT TATTCACTCC 1140
AAGGAGCCCA CAGGCCTCTT GCCTTCAAGA CAGTGCTGCC CTGGACTCCT CAGCCCGGGC 1200
ACTAGAGACC ATTCTCTCCA TCTCAGTCTC TGTGCTGGGG CTGGGACAGC ACCCAACACA 1260
CCCTTGCTGC ACCCAGGCGT CTCACCCACC CCTGCCTGCC TTCAGGCCCT ATTTGATCTC 1320
ATCTCCTCCA AGGCCCTGAC CCTCCCTCCT CTGAGCATCC CCTGTCCACT GAGGCCAGTT 1380
TTTTCTGGTG TCTTTTCTCC 1400
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