| Tag | Content |
|---|
EnhancerAtlas ID | HS133-22953 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr3:129314340-129316420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr3:129315008-129315018 | CCCAATTAGC | + | 6.02 | | Zfx | MA0146.2 | chr3:129315150-129315164 | CTGGCCTCGGCCTG | + | 6.07 |
|
| | Number of super-enhancer constituents: 33 | 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_31151 | chr3:129314599-129316987 | Fetal_Thymus | | SE_31569 | chr3:129313699-129319812 | Gastric | | SE_33524 | chr3:129314769-129317750 | H2171 | | 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_46996 | chr3:129313726-129317137 | Ovary | | SE_47266 | chr3:129310010-129324076 | Panc1 | | SE_48609 | chr3:129310376-129325641 | Right_Atrium | | SE_49818 | chr3:129314283-129315255 | Right_Ventricle | | SE_49818 | chr3:129315309-129316984 | Right_Ventricle | | 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: 4 | Chromosome | Start | End |
| chr3 | 129314620 | 129314813 | | chr3 | 129314978 | 129316172 | | chr3 | 129315034 | 129315445 | | chr3 | 129315678 | 129315871 |
|
Enhancer Sequence | TGGTCAGGAA GCCTGGCCTT AGCCACAGAG GAAAAGCAGC CTGGAGGAGC ACGTTGGAGA 60
AACCAAGGCA CAGAGAAGAG CAGAGGCTTC AGACAAACGG CAAAGGACAC AGCAGCTCTG 120
GCAGACCCTT CGGGGAGGCC TGCCTTGGTT TCCCTGACCC CTCTGGAAGA GGCGGGTCAC 180
CCAGCTCCAG GGCTTTGAGG TTATCCAGAC CAGCTGGACA CCATCTGGAA GGGCTGAAGC 240
CAGCCAGCCA GGCCGCCCTG AGGGCCAACA CACAGACTGG GCATGATCTG CCCACCCACC 300
CCAAACAGGC ATGGCCTGGA AGGACAAGCC CCAGGCTTAG GTCACAAGCC TGGCTGGATT 360
AAGGACCTAC TGTGTGACAC TACAGCTACT GGGGGCACCT TACAGCCCTG GGGGTGCACG 420
CACGCACACA CACACACACA CACACACACA CTCTTGCTGC GTACCCATTT TACAGATGAG 480
AAAGCTGAGG CTCCTGACTC CTAAGTCTCA CAGCTCTTAC CTCACTATGG GAGGCACCAT 540
CCCCTCTGAA CCTCGGACTC CACATCTGTA AAATAAGACA GCAATAGCAC CCACCACCTA 600
GGGCTTATGG AAGGACTGAG CTCATAGGAG CCTTCAGTGC TAAGCACTGT AGGTGCTCAA 660
TAAATGTTCC CAATTAGCTA TGCAGACCAC GGAGCAGAGG CTCGGGAGCT CCCGAGGACA 720
GGGACAAGCC ACTCCACCGC TTCCTGAAGT CAAAGCATCC GAGGCTGGAT GGGCTACACC 780
GCCCTCACCA AGGACACAGT AGTGGGAGCT CTGGCCTCGG CCTGCTCTGC CCTGGCGCCT 840
GGGAACCACC GCCACAGTCG CTGACTCAAG CAGCCATTGT TTAGTTAGCT GGACGCAGCC 900
CCTAGACACC CAGCTCCCCC TTCATGAAGC TGTTTCTCAT TCCGGCCCGG CCTGGCCCCA 960
TTTCCAGCTC CCCTCCCCCT GGGTCCCAGA GGAGCACAGT GTGGGATGGG CAGCCAGCGG 1020
CTCTTCCCTG GCCCAGGGAA AAGGCTTCCC TCCCCCCAGC AGGAGGGGCA GAGCACGAAG 1080
CCAGTCTTTC CAAGCCCTGG AACAGTTTCC CTCCCAGCTT CCTCCCCTGA AGGGACTCCA 1140
GGCCAGGAGC CGAGAAATAG TTGCCTCTCC AGGGAACACT GGCAGTTCCC TCCTGGGGCT 1200
GGGGGGACTT GGAGGTTCGA TCTCACACCC TCCTCCCCAG CCCCTGGTCT CCTCGGGGTC 1260
CAGCCCATAT GCCTGGCCGC AGGCTGTGCT CTGCAGCAGG ACTCTACCGC TGGTCCCAGA 1320
GTCATCGCAC GACCGCTGTG GACACAGCCA AGAAGACAGG GCTGCTTGGA GCCTTGCGCA 1380
AACATCTCCG GGCTGGATTC CATGAGCTGG GGACACAGAG GTGACAACGG GGCCCTCTCT 1440
CCAGCTGCCC ACATCCGAGC TCAGAGGCCC AGCCCCAGGA TGGGGAGGGG CAGCTTTCTC 1500
ATAGTAACAG TTCGGTAGAG TGACAGTAGC AAGCAGCTGT GTGCAGTCTG CTTTGTGCTG 1560
AGACCTCTTT CTGTATTATC TCATTCAACC CTCACCACAC CCTGAAAGAG TTGATGCTGC 1620
TTTACAGTAA AGGAAACTGA GGCACAGAGA GTTGAAGTGA TTTGCCCAGG GGCACACAGC 1680
CGGAATGGCT AGATCCAAGC CTCCAGCGCA GGCCTGCGGG CTCCAGATCC CCGCCCTTAA 1740
CCACAGCCTC CCCACCCGCC GCTCTGCTGG GAGCCACCAA TGGTTGCCAG GAAATCAGCC 1800
GCTTGGAGCT GGAAAAACCC TGGGTTTTGA GCTGGGGAAA CTGAGGCCCA TCAAGGTGAT 1860
GGCTGCTTCT AGAGAGCTCA GTCACCTCAA ACAAAGATAG CGGGCAGAGG CTGGAGAAGG 1920
GCACAGGCAA GGGGGTTTGG CCACTTTCCT GGGCCTGGCC TCCACTCCAA GGCCTCTGCC 1980
TGCGGGCCCC CCCCCATTAT TTACCGATCA GAGCATAAAG TGCTACATGA TTAACGCCCC 2040
ACTGGGGCCT TGCCGGGACT CGTAATGGAG CTGCGAGCTT 2080
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