Tag | Content |
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EnhancerAtlas ID | HS176-07914 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr11:95991190-95993760 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
DUX4 | MA0468.1 | chr11:95993142-95993153 | TAATTTAATCA | + | 6.62 | Foxd3 | MA0041.1 | chr11:95991514-95991526 | AAATGTTTGTTT | + | 6.27 | Gfi1b | MA0483.1 | chr11:95991686-95991697 | AGCTGTGATTT | - | 6.14 | IRF1 | MA0050.2 | chr11:95991347-95991368 | TTACTGAAAGTGAAACTTATA | - | 6.64 | IRF1 | MA0050.2 | chr11:95991563-95991584 | AGAATGAAACTGAAAGAGGCA | - | 6.76 | IRF2 | MA0051.1 | chr11:95991351-95991369 | TGAAAGTGAAACTTATAA | + | 6.4 | IRF8 | MA0652.1 | chr11:95991350-95991364 | CTGAAAGTGAAACT | + | 6.19 | RREB1 | MA0073.1 | chr11:95993345-95993365 | TGTTGGGGGATGGGGTGGGG | - | 6.61 | TBP | MA0108.2 | chr11:95992060-95992075 | CCCAGCCTTTTATAC | - | 6.22 | ZBTB18 | MA0698.1 | chr11:95992404-95992417 | TTTCCAGATGTTT | + | 6.28 | ZNF263 | MA0528.1 | chr11:95993349-95993370 | GGGGGATGGGGTGGGGGGAAG | + | 6.1 |
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| Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
SE_00421 | chr11:95990695-95994185 | Adipose_Nuclei | SE_09528 | chr11:95988993-95993093 | CD14 | SE_10685 | chr11:95986205-95993908 | CD19_Primary | SE_11167 | chr11:95985208-95994550 | CD20 | SE_12380 | chr11:95989202-95994108 | CD3 | SE_15173 | chr11:95986487-95994286 | CD4_Memory_Primary_7pool | SE_16197 | chr11:95990631-95994008 | CD4_Naive_Primary_7pool | SE_17498 | chr11:95985112-95995021 | CD4p_CD25-_CD45RAp_Naive | SE_18301 | chr11:95989089-95994399 | CD4p_CD25-_Il17-_PMAstim_Th | SE_30644 | chr11:95990730-95992362 | Fetal_Muscle | SE_31211 | chr11:95989224-95993674 | Fetal_Thymus | SE_36675 | chr11:95990838-95992393 | HMEC | SE_36675 | chr11:95992462-95993458 | HMEC | SE_44431 | chr11:95990759-95993077 | NHDF-Ad | SE_45599 | chr11:95989581-95994498 | Osteoblasts | SE_50559 | chr11:95991362-95993946 | Sigmoid_Colon | SE_53120 | chr11:95991353-95993089 | Small_Intestine | SE_54051 | chr11:95991340-95993046 | Spleen | SE_54051 | chr11:95993137-95993909 | Spleen | SE_58447 | chr11:95917840-96001635 | Ly1 | SE_61108 | chr11:95917662-96027831 | HBL1 | SE_61760 | chr11:95940172-96001818 | Toledo | SE_62369 | chr11:95920962-96006907 | 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 |
GH11I096253 | chr11 | 95986252 | 95993991 |
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Enhancer Sequence | ATTAATTTGG AACTAAATGC CTTTAATTTT TACCGTGATA GGTTTGTGGC TCTTGACATC 60 TTTTGGTCCT ATTCATCAAA ATCATTTGCT AAGTCCAAGG TATAGCAGAG TGGCTTTAAC 120 AACAACCATG GAGGATGAAT AAAATACATT TTCATATTTA CTGAAAGTGA AACTTATAAG 180 CATATATCAT CTTCTGCCTA CCTTGTAAAT ATCCCATGTT TTCATTTACA TATTGTACCA 240 ATTAATATAT CTTGGTACTA ATCAGAGTGG AATCCACTCC TGACATGGGA GAAAACTACG 300 ACAAAAAACA TTAGCAGCAA GAAAAAATGT TTGTTTCAAG TATGTGGATT ATATTTTCTA 360 GTGCCTTAAA AAAAGAATGA AACTGAAAGA GGCAGCTTGA AGAAGCTTAC ATGTGTTTAA 420 AACCCACATC CTGTTGTTAT CCACTGCCCT GGCACAGAGG AGCTGGGAGG TGAACGTCCT 480 CATTAGGGTC CCTATTAGCT GTGATTTGCA ATGGGCTTCT CCAAAGAAGA AAATCACATT 540 CACCCACTGG ACAATGGCCC AGGTATCACC ATTGATGGGA ATCATATATG GAGTAAACAT 600 CAAAGCCCAA GAATACAGTG GTCTAAGCCA GTGTGCTTAG AAGTTGCCAG ATCCTCCATG 660 CTTCATTCCA GCCACTATCA GCAGATTCTA AATCACCTAT GAGCAGAGAG GCCCATCTGC 720 CTAGGGCATA AACGAAATTA TAACAACAGT GAGAGAGCCA ATGGGAGTCA GCCAGTAAGA 780 CTATGAGCAG CATGATGTAC TCAGACTTTT GTTCCTTTTT ATTTATTTGG TTAAAATACA 840 TGTGTTTTTG CTTCAGGCAG ATGTTGGTAT CCCAGCCTTT TATACAGGAA GCTGTAGAAG 900 GGAGAGGACT TTCTGGGTGG GAGCAACTTA TTGTGGAGGC CAAATGGCAT TTTTTGTAGG 960 CCCTGAGATT TTTTACGAAA ACACTAACTC TGTTCAGAAC TCTTTCAAAG GGTGAAGACA 1020 AACTTAACAA CCTTATACTA TAATACAAAT AATTACAGAG TGTTGCTTTA AACTTGTATC 1080 TTGAAGTTCC TTCTTTAGGT AACTCTGCTT AACAACCACA GACTCTTCTT CCTAATGGCT 1140 TATCTGCATG TCTTTTCAAT TTTCTAAGTG AAGGCCAGCC CCCTTCAAGA TGTTCTACCA 1200 ACTCAGTCCT ATTCTTTCCA GATGTTTTTT TTCTTTTTCT TCTTCTGAAA AGCATGTGTT 1260 GATAGACTAT GGGGAACAGA CCAAGATTTA TTTTTTAGCC AGCATTTTCC CCTTGCAACC 1320 GTAAGTCATT CTTCCTCAGA AGGCAAGGTG GGGCAAGTGA TTCTAATGTG CTTCGCTCCA 1380 ATGCTTCCAT CTCAATAACC CTTTAAAGTG AAAACTGTGG AGAGTGAAGT GAAAAACTTG 1440 TCTCCATCTG GAAGCATTTA TACAGAGAGG TGTCTTTAGC TTAGTTGTTT GTCTAGAATT 1500 TCCATTTATG AACCGACTTG CCTTTCTCCT GTGGGTATGC TGGAGAAAAC TCTTTGCAAA 1560 ATCCATTGTA TGCAATAATC CAGTGGCTCC TTCAAACTCA ATCAGGCTGG AAAGGCTAAA 1620 TATGACTCAT AGGATTCCTC CAACAAACAC AAAGTAAGTC AGAAGTCAAG GAGAGAGTCA 1680 TCTCGATGTG GACCAGCTTA CCTAGCAAGG CAGGGAATTG TCATAAAACC AGTTTCCTGC 1740 TTGCAAGACC TTGACTCCTT TCAGTAAAGG TGTCAACTCT TCTTTTTCTG AACAATCTCA 1800 ATGTGAATGA CAGGGCCTGA TTCTAGAGGA AGGTGTCTTT AATCTTTTTA TGGTTCAGTA 1860 TAAAGGTTAC CTTAAAAAAA GCCTTGGGAT ATACTTTCAA GATACTGACT TGTGATTTTT 1920 TTTTTTTTTT TAAACATCAG TATGTCCTGT TCTAATTTAA TCATTATTCT TTCAAACAGG 1980 CTGGGAGGAA AGGTTCCTGG ACATCCACAG AGAAAACTTA TTCAATAAAA CATTTTATAA 2040 TCCTCGGAAC ACCTGTGCCA CCTTCCTAAA GGCCAGTCAG TTCCAGGACT TCCTAAAAAT 2100 GAAGGTTGGA CTGTGTGAAT GCCTGTGTGT GTGGGAGTGG AGTCACTCTG TGTGGTGTTG 2160 GGGGATGGGG TGGGGGGAAG CAAACTGGCA GACTCTAGAA GGATGGTGGT AGAGCAGAAG 2220 AAAAAAGAAG AATGTCTGAA TCTGGAGTGG CCCCATGAGA CCCAGTCTGT ACTCAGGTGA 2280 CACTGGAATA ACAGGAGTTC CTTCTAAAAC CAAGAGAGCA GCAGACACTC TGTCATGCCA 2340 CACCCTTCTC AACTGTCTTA TCCCTTGGCC GTCTCCTTTT TAGAAGCTAA AGCAATACAT 2400 TTTTTTCTTC AGTGTCTCTT GTTCTTGGAA TGGAGGTGCA GCATAGTTCC GGCCAATAAG 2460 ATGGACATCT GATAGGAGAG GGGTGTGCTT TTGGGACACT TTCAGCTTTT CTGATAAGAG 2520 GAACACCAGG GCTGCCCTCA CTCCTCCCTC CAGTCTGCCA ATGTGATACC 2570
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