Tag | Content |
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EnhancerAtlas ID | HS038-00252 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr1:21667000-21668250 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LMX1B | MA0703.2 | chr1:21667338-21667349 | TTAATTAAATT | - | 6.32 | Lhx3 | MA0135.1 | chr1:21667335-21667348 | AAATTAATTAAAT | + | 6.07 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_00105 | chr1:21656775-21671990 | Adipose_Nuclei | SE_00854 | chr1:21663168-21667245 | Adrenal_Gland | SE_00854 | chr1:21667352-21672486 | Adrenal_Gland | SE_01643 | chr1:21663301-21667219 | Aorta | SE_01643 | chr1:21667344-21672121 | Aorta | SE_02944 | chr1:21666135-21667266 | Bladder | SE_02944 | chr1:21667360-21668291 | Bladder | SE_05710 | chr1:21667990-21673560 | Brain_Cingulate_Gyrus | SE_05944 | chr1:21659989-21673592 | Brain_Hippocampus_Middle | SE_08398 | chr1:21667381-21673694 | Brain_Inferior_Temporal_Lobe | SE_26127 | chr1:21667455-21671889 | Duodenum_Smooth_Muscle | SE_26770 | chr1:21663415-21667226 | Esophagus | SE_26770 | chr1:21667319-21672743 | Esophagus | SE_28486 | chr1:21667334-21672947 | Fetal_Intestine | SE_29337 | chr1:21667313-21673152 | Fetal_Intestine_Large | SE_31433 | chr1:21663236-21672659 | Gastric | SE_39164 | chr1:21667486-21670213 | IMR90 | SE_42174 | chr1:21667300-21672712 | Lung | SE_46660 | chr1:21664031-21667287 | Ovary | SE_46660 | chr1:21667360-21668323 | Ovary | SE_47592 | chr1:21667472-21668246 | Pancreas | SE_48583 | chr1:21663300-21667219 | Right_Atrium | SE_48583 | chr1:21667258-21672989 | Right_Atrium | SE_50108 | chr1:21663357-21673470 | Sigmoid_Colon | SE_52633 | chr1:21663378-21667298 | Small_Intestine | SE_52633 | chr1:21667302-21672599 | Small_Intestine | SE_53334 | chr1:21667327-21672651 | Spleen | SE_54639 | chr1:21663094-21674002 | Stomach_Smooth_Muscle | SE_65263 | chr1:21660486-21671744 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 21667000 | 21667175 | chr1 | 21667362 | 21667447 | chr1 | 21667607 | 21668150 |
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Enhancer Sequence | AGAATGCAAA TCCGACCGTG TCACTCCCCT GACTCTAAAC TCCTCAGTAG GCTGGGTGCG 60 GTGGCTCACA CCTGTAATCC CAGCACTGTG GGAGGCTGAG GCGGGTGGAT CACTTGAGGT 120 CAGCAGTCCA AGACCAGCCT GGGCAACATG GCGAAACCCG GTGTCTACTA AAAAAATACA 180 GAAGTTAGTC GCATGGTGGC ACGCCTGTAA TCCCAGCTAC TCGGGAGACT GAGGAGAATC 240 ACTTGAACCA GGGAGGCTGA GGCTGCAGTG AGCTGAGATT GCACCACTGC ACTCAGCCTG 300 GGTGACAGAG CAAGACTATG TCTCAATAAA TAAGTAAATT AATTAAATTT AAAAAATAAA 360 CTCCTGAGTG GCTCCCCACT GCCCTAAGGA TTGAGCCCCA GGTCCTTCAT ATGACCATCC 420 CTGAGTGCAC CCTCCGGGCC ACCTCCTAAG CACAGTCCTC CGTGCCTCCA GATGAACCAT 480 CCCTGAAGGC ACAGCGGTCT GTACTCTTGC ACATTCTGCT CCCTCCACCC CCCGCCCCCC 540 AACACTCTTC CCAGTCCCAC TCGCTCTTTA GGTTATGATT TTAATGCCAT GTGCTCAGGG 600 AGCCTTTTCT GATCCTCAGG TCAGGTTCCC GGTCCAATCC CACAGCCCCC CGCGTGTCTC 660 CCTGACAACA GTAATTGCGC TTGTAATTTC CTGCTCTGTA TCTGTCTGCC TGCCTGTCCA 720 TCAGACTGTG GGAGAGAGAG ACCTATCAGT CTCACTCACA CTGACCACGG CCCCCATGCC 780 TCGTGTTGTG CCAGACAGAC TTGTTTGGTG AGTGAGTGAA TGAACAAATG AATGAAGCCC 840 TTTGACTATG GCAGGAGGCT TACCCAGTCA ATTGGAGAGA AAAAAATTGA GCAGAAGCAC 900 AAAAAATTGT AAACATTTGC TCATGGTTCC TCTCTCACCG TAGACATGAA AGTGTGGACT 960 TGGCCAAGCT GGTTTTCTGG GCTAACGCCC AGAACATTCT GCCAAGCCCA CCTTGTAGCC 1020 CTCTCATGCC TCAAATCCTG TTCTTCCCCT GGCCTCCCCA ACTCTGCAGG GAAAACAATG 1080 TATTTATTCT TTAACAAAAG GTAACAACAT CCTTGTTTAC CAAAAGAGTG TAGCAATGTA 1140 AGGAGGCCTC AGTAGCCCAG TCACCAGCAG GGGCACAGGC TGCCCAGGGT GAAGTACGCA 1200 CTGTGCTCTG GGAGCCCCAT CTGGAGTGGC TGAGAGGCAC CAGAGTGACG 1250
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