Tag | Content |
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EnhancerAtlas ID | HS170-02658 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr3:46993740-46996190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFAT5 | MA0606.1 | chr3:46994097-46994107 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr3:46994097-46994107 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr3:46994097-46994107 | ATTTTCCATT | + | 6.02 | ONECUT1 | MA0679.1 | chr3:46994252-46994266 | AAATAATCAATAAT | + | 6.41 | ONECUT2 | MA0756.1 | chr3:46994252-46994266 | AAATAATCAATAAT | + | 6.65 | ONECUT3 | MA0757.1 | chr3:46994252-46994266 | AAATAATCAATAAT | + | 7.08 | Six3 | MA0631.1 | chr3:46995895-46995912 | GTAAATGATACCCTTTC | - | 6.49 | Zfx | MA0146.2 | chr3:46996175-46996189 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_11155 | chr3:46992916-46999427 | CD20 | SE_13638 | chr3:46994762-46995520 | CD34_Primary_RO01536 | SE_16650 | chr3:46995196-46996197 | CD4_Naive_Primary_8pool | SE_18708 | chr3:46994025-46999175 | CD4p_CD25-_Il17-_PMAstim_Th | SE_20061 | chr3:46993290-46999305 | CD56 | SE_22640 | chr3:46993292-46999309 | CD8_primiary | SE_23114 | chr3:46995344-46995948 | Colon_Crypt_1 | SE_23749 | chr3:46995423-46995698 | Colon_Crypt_2 | SE_31407 | chr3:46994963-46996170 | Gastric | SE_32585 | chr3:46994064-46996580 | GM12878 | SE_40617 | chr3:46993326-46996283 | Left_Ventricle | SE_42118 | chr3:46993348-46996243 | Lung | SE_48684 | chr3:46994207-46995085 | Right_Atrium | SE_48684 | chr3:46995270-46996230 | Right_Atrium | SE_52388 | chr3:46994262-46996004 | Small_Intestine | SE_53507 | chr3:46994588-46996144 | Spleen | SE_58746 | chr3:46966845-47032612 | Ly1 | SE_59412 | chr3:46966960-46998383 | Ly3 | SE_59747 | chr3:46966600-47033537 | Ly4 | SE_60850 | chr3:46965041-47030117 | DHL6 | SE_62445 | chr3:46966331-47033109 | 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 |
GH03I046952 | chr3 | 46993692 | 47003318 |
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Enhancer Sequence | ACAGGAACTT CTGTTGTGTG AGCCTTCCAA CAGCACCCAC GTATTCGGTT ATCACTAGCC 60 TTGTTGCACA GATGCAAGAA CTGAGGCTGG ACCAGGTCTG TGCATGTCAT ACCTAATACT 120 CTTTCCATTG GGTAGAGCAC AAGTTTTGGG AAATAAACAG AAGCCCAGCT CCCCGCTGCC 180 ACATCCTCAG TTCTTTCTAC CACACATGCT GCTTGTTTAT CCTTTAGTTG TCTGTTCTAT 240 CCTCTTTTCC AACAACTATC TGCACCTCTG CTTCTCTCCT GCAAAATGAA GACAAAAATC 300 CCAACCCTGC CCACTTCTTG GGAGTGTGGT TTTAACTAGG TTCCATAAAA TTGGAAGATT 360 TTCCATTAGA AGGTGAGCCC TGGGCAGTGC CGAACCCAAA TGTCACTCTT CTCTGTTCTG 420 CATGTCTTAC AACACTGTCA ATTCTTTGGT AATAACAGTA TGCCAGGCAA CTGATTATTC 480 CATTAATTAA ACAGTAGTAC TGATATTATC AAAAATAATC AATAATTAAT CACTATGAAA 540 ATCTAATAAG GTCAGCACTC CTTTCTCCTA CCACAGATGA GAAAAATGGA AGCCCAGGAC 600 AATTAAGTAA CCCATCCAGA GTCACACAGC TAGAGGTTGC CAGGACGCAA ATGGCAGGGC 660 AGGCTTCAAG CATAGGCTGA TTCCCTCTAG AACCCCTGCC CTTTGCTCTT GTCCCACTCC 720 TGTCCCTACC TTTCACATGC AAATGGTTTC AAGTGTGTCT AGGGTGCCTC CATCTGTCAT 780 CACATGAGAG TTGACAGCTC TTTCTGGTGT CATTTCAGAG AGATACAATC AAACCCATCG 840 AGAGCCCCAA ATATTGTCAT TTCTTGGCCA AGAACTCCAG TCCCAAAAGA CATCACAAGG 900 AAATAAAAGA GCAATGCATG CAGAGGTGTT TAGAGCTGTG TTTCTCACAG TAGGGAGAAG 960 TGGAACTATG CAGTGAGCCC AACACCGTAG GGCACAGTTA TGCAGGCCAG CATTCACATG 1020 ATGGGCCAGG GGAGGCATTA AAATAGCGAG GCAGCACTAT GCAACAGACA AACACACAAA 1080 CGCCAGGGGT AAGAGTCCTA TATTACATAC TCATGATTGC AACCATGGCA ATACCATACA 1140 TACAAATGGC CAAAGACTTC ACAGACTCGC ACTCAACCGT GGGTAGTATT TTTTCCATCT 1200 TCCTTAATTC TGCTGTCAAA ATGACTTAAT AATAAAAGTA ACCAGAGGAA CCTAGCTGAC 1260 TATGGCTCAC TATCTTGACT CATACCCTAA ACAGATTCTC TTGACCCTCA CCTGGCTAAA 1320 TGGGGAAGCA GGAAACCATG GCTGGCACTC AGGCCTGACA CAGCCTTGTC AATGCCTAAT 1380 GACTTTTCTC AAGCTTGGAA AAAAAAAAAA AAAAAAGTCC AGCTTTGCTG GTGCAGAAGA 1440 GGACAGGTTG AGCCTGCACA CACCAGCGTC CCTCTGCAGC CTGGGACTCT AACCACAGTA 1500 GCAAATGCAG CAGCCAATTG TAGACTAAGC CCTCTTAAAT CAGGATAGAC ATCTCCATTA 1560 CTGGGGGGCT AAAAATGTCG GTTAAGAAAC TAACTGGTGA TGAGCAATGA AGTCACCTCC 1620 CCACCCTCTC ACCCTACCCC ACCATTTCCC TTTTCTTGGA GGGGAAAAAA GCCTCCTTCA 1680 CCACAAAGCA GAATTCACAA CCACTAGGAC TTCCTCACCA TTCTAAGCTC ACGAGGGGAG 1740 CAGCAGTGAG CAAATCACAA AAGCAAATGA TAAGGTCCAT GCAGATTGGA AGACCCCTCC 1800 CCTGGTGGGA GACAGCTTCG TGTGGCACCC AGAAACCCCT TCCCCATTGC CTCACAGTGG 1860 ACAGTCAGAG GAATCAGGCA CAGGGGGCCC ACCTGGTCAG TTCCAGGGAC TGGAACAACC 1920 ACCCAGACTC TCTGGTCCTG AGGACATGTG GCTGCTACCT GACCATCCCC AGATCTGTAA 1980 GGCCTGTAGA ACAAAAGAAG GTGACCTTTC TCCACAAACT CTGGCTGGTA GATAGGATCC 2040 TTAGGCTGAG CCCAGGAGGG AAGAGGAGGA GAAAGCCCAA CCACTATGTG TTCACTTTCG 2100 CTGGATCCAA CAGAGACAGC AAGCAAGGAC CTGAAAACCT CAGTGGGTGG CCCCTGTAAA 2160 TGATACCCTT TCGCCTCCCA CACACACCCT AGTCCCATGG CCCTGTTTAC ATCAATTCTG 2220 GATCCCCTAA AACAGTTTCC TTGATAGCTG CCAACGGCCC TCACTCAAAC CTGGCACCAG 2280 ATGCATCAAC CTCTATAGCA TCTATGTGAC CTTTCATGTG GGTAGATTTG TTCTTAAAAT 2340 GGGGTGGGTC AAGGGAATAA GAGCTACCAT TTATTAAAAG AACAGGTATT TCCACCGGGC 2400 ACGGTGGCTC ACGCCTGGTA ATCCCAGCAC TCTGGGAGGC CGAGGCGGGC 2450
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