Tag | Content |
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EnhancerAtlas ID | HS050-06121 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:226909850-226912880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:226911530-226911542 | GATTGTTTTTTT | + | 6.44 |
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| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00103 | chr1:226910268-226914123 | Adipose_Nuclei | SE_03869 | chr1:226909642-226914235 | Brain_Anterior_Caudate | SE_04801 | chr1:226909769-226913572 | Brain_Cingulate_Gyrus | SE_05781 | chr1:226909371-226914464 | Brain_Hippocampus_Middle | SE_06710 | chr1:226909842-226916981 | Brain_Hippocampus_Middle_150 | SE_07746 | chr1:226909997-226913021 | Brain_Inferior_Temporal_Lobe | SE_10887 | chr1:226909951-226923692 | CD20 | SE_11833 | chr1:226909764-226911682 | CD3 | SE_14432 | chr1:226909851-226912708 | CD4_Memory_Primary_7pool | SE_16856 | chr1:226911061-226912520 | CD4p_CD225int_CD127p_Tmem | SE_17296 | chr1:226909602-226929357 | CD4p_CD25-_CD45RAp_Naive | SE_17765 | chr1:226909495-226928628 | CD4p_CD25-_CD45ROp_Memory | SE_18263 | chr1:226909481-226929370 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19160 | chr1:226909740-226917128 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20012 | chr1:226910259-226912653 | CD56 | SE_21455 | chr1:226909788-226913136 | CD8_Naive_7pool | SE_21910 | chr1:226909778-226912096 | CD8_Naive_8pool | SE_22315 | chr1:226909647-226920088 | CD8_primiary | SE_25774 | chr1:226910377-226912751 | Duodenum_Smooth_Muscle | SE_26570 | chr1:226910465-226912445 | Esophagus | SE_31634 | chr1:226911457-226912281 | Gastric | SE_40782 | chr1:226909759-226913910 | Left_Ventricle | SE_42228 | chr1:226911370-226913154 | Lung | SE_48643 | chr1:226911574-226912796 | Right_Atrium | SE_50140 | chr1:226909756-226911426 | Sigmoid_Colon | SE_53341 | chr1:226910761-226911343 | Spleen | SE_54498 | chr1:226909687-226917100 | Stomach_Smooth_Muscle | SE_55112 | chr1:226910349-226911054 | Thymus | SE_58303 | chr1:226819953-226937809 | Ly1 | SE_59629 | chr1:226819233-226928465 | Ly4 | SE_60416 | chr1:226819368-226929640 | DHL6 | SE_62233 | chr1:226813614-226929647 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I226722 | chr1 | 226910218 | 226912514 |
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Enhancer Sequence | AAAGTCAGTG TTCCCAAACT ACAGTCAGAG GCCAGGCTCA AGGTTCCTAG CAACCTGCCA 60 CCTGGTACAT TCAGGGCACT CGCCCTTCAA GCACAACATG GATCCTTGGG GCTCCTTGCC 120 ACTCCAACTC CTAGGAGACT CTCCTGCCTT CCCCTGGGAA TGTGGTATTT GAGGCCAATG 180 GTGACTGACC AGAAAATCTA GGCCAGTTCA AAATGCCAAA GACAGGATGC CAGGAAGGAC 240 CCAGAACCTG CAGGGCTCCG TTCAGCTTCT TGGGGTTAAC CAGCAGTCTG CAGAGGCGGG 300 AGACGGCTCG GCTCTCAGGA GAGAGCAGCT GATTTTTAAT GTACAGTGTA ATACCGCAAG 360 GTAAACAGCA TCCCAGACGC TGCTCCATAT GGCTTTACCC TGAGATCGAA ACTAATTACC 420 ATTCTGTGTA TATTTCCAGG TTGGGGCAAT AAGGGAGTTA CTGTCCAGCA CATTCGCCAT 480 CAGACCACCC CTGAGGTCAA CACTGCCACG TGCTAACAAG CTCCTTTCGT GGTTTCAATC 540 CTCCCAGACA TCAGTCCCTT CATCCTGCAA AGGGCAGAAA GAAACTGGGG CTTGGGGAGG 600 TGTTAGGGCA GGCTGAGCCT GAGACACATA TGTCTAGAAA GGGGCAACGT CTCAAAACTG 660 CACATTCAGA GCCTGGAAGC TCTGTACAGA TGCCTAATGG GTCCTGGGGC TAGAAAAGGT 720 TTGAATAGAT CATCCTGGAC AGAAAAGATG CAAACCCCCA GGGGTCAACC CTGCAGGCTA 780 CCTGCTCCCC CTGCCCCCCA CCCATTACAG CTGAAAGGAA GGAGAGAGTT CCATTTCACA 840 CATCCTGTGT GTAGCAGAGT AGAGACCAGG GTTTGGCAGG CAGGATGCCC AGGGCTGTGG 900 TGACGCCAGT CCGTGCTGCT CAGATGGAAC CTGTAGCCAT CCAGCCCGGA TCCTGCATGG 960 GTTCCAGTAG GCCCTCCTGG GACTTGGAAG TGAGCTGGTG TGCTCGGGGT TCATCAGCTC 1020 CGTCCAGTCA CCTGACTGGC TTTTCCTTCC ACTCCACCAT CCCAGCCCAG ATGACAAGGG 1080 CACAGTATGG CCTTGTGACT TGGGAAGTCC TGGGTAGGTT CTCTGTGGCT CACTTCAAGA 1140 GGAGGCCAGG GTGACGCACA GTGTACTTCA GAGACCCCAG AGCCACCTGG ACCTGAGTCC 1200 CTGTGAATGG ACACGTGACG GGCCTCACTG GGTGTGCAGT AAGATAAAAC ATCTCCTTAA 1260 TCTCAGAGAG AGCCTGTGTT AATAAGCACG TGCCTGGCCT GGCACCAGAT GCGGCACAGA 1320 GAAGAGACGA AGACTAATTA AATCACACAC GTCCAGAGAC CTCCTTGGTA AGAAAAGCCA 1380 CACCGATACA GAGTAGTGTT GTTCTACACA CACACGTGTG TGTGGGTGTG TGTGTATAGA 1440 GAGATATATA TGTATATATT TCATTGGCTC TCTTATGAGC TACAGTGACT CTAAAAGATG 1500 CACCAAGAAA GCAGAGGAAC AAGGGGAAGG GAGGGAAGGG ACAGAGGCTT TCACACCCCA 1560 AATGCTGGGC ATTTTGTGTC TGGATGACCT CAGCCAGTTT CCACCTACAA AACAGAATAA 1620 AAAGAGGCTG GTCCCCAGGG TGTGTAACCT GACACCTCTT GCCGGCAGCT GAATACAGGG 1680 GATTGTTTTT TTAAACTTCA AGTTCCAATC CCTAGTAACA AAGTGAGGCC TCTCCTGCAA 1740 CTAAAGAACC TCCCTGGAAA AATAAATCCT GCTGCCTGTT TTGTCATCAT CTTCGACAAT 1800 TAGCTGTACT TGGGACAACG TGACTCGAGC CAATTGGTGA AGGCGATTAG GGCATCCACT 1860 TAAAAACGCT CTTCACAACT GGTGGAGGGG TGTCCTCTAT TCCACCCCTG TTCTGCACCC 1920 GGTACTTGAG CTGCATTATC TCCTTTCATC TTCACAGCAC CCCCTGAGAG AGGCTCATTA 1980 TCCTCATGTT AGAGATGAGG ACACTGAGAC TCAGAGATGT TCAGCCCACG CCAAGGTCTA 2040 GGACAGAGTG AGGGTGTGGG TTCAGGTCTG GCTGGCTCGG GCTCCACACT CCCCAGCAGA 2100 CCATCTTGCT TCTGTGCTCA GCAGAGCAAG CCTCCCCCAG CACACACTTC CTACAAACCT 2160 CAATGTCAAA GAGCTCCCAG ACCCCATGAC TTCTCCTCTT CCAAGGGAAG AAGTCAGCAA 2220 CACTGCCTCA GACACCCTTA TTCACTCTCA CCCAATCAAA GAGAATGGTG GAGGTCGCAG 2280 GTTCGGCATA AAATACTAAC AAATGACACC ACAGCTGCCT CTGAGGTCCA TGCTATTGTA 2340 TCGAGCATTT AGTATGTCCA GACGCTGTGC TAGGCATTTC CCACATTACC TTGTTTAAGG 2400 CTCACAGCCT TAAGGTGGGT ATTATCAGTC ACATTTCACA GATGATGCAA CTGAGGAGCA 2460 GAAAGTTTTC TCTAGGGTCA CACAGATAGG AAGTAACAGA GTTTAGACTC AACCCAGGAC 2520 TACACCTCAG GGTTCTTCCC CTCCCCCTAG AGCTCTTCCA TAGCTAAGAC TCTATAACGT 2580 GTACTAAGCA GAAAAACCCC TGCCGAGCTC TCCTGACCAT GTCCTTCTGG TCAATCGGGG 2640 TCCTCCCGAG AGCATAGCAA CAGTGCAGCT GACTGGGCTC TGCACCGTGC AACTGCTGAG 2700 CATCAATTTG TGCAGAATCC AACGCTCCAA ATCAAGTACT GGGGCAGGGG TGCCCTCTTT 2760 CATTCCAGCC TCCGTGAGCC TCTGGATCCA GAACAGTCTC TTTGATCTAC CACTTCTAAC 2820 AGAGGGAGCA AATTCCTCAA GACCTTTACC CCAGACTCCT TCCCTAGAGG CTGTTGCCCA 2880 AATCCAGTTC CTTTACTCCC TGTTCCACAA CATGTACTGA AGCTTTCTGC ATTGTGCATG 2940 CCAGCACCAA CCCATTATTT GTTAACTCAT ATTTAATGAA CATGCTTGCT CAATGGCCGT 3000 ACAACTTGTT CTTCAGTTTC ACAAATTTCC 3030
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