| Tag | Content |
|---|
EnhancerAtlas ID | HS187-20209 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr5:150476340-150479530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr5:150479175-150479193 | AGAAGAAAGGAAGTAAAG | + | 6.04 | | IRF1 | MA0050.2 | chr5:150477986-150478007 | TTCTGCTTTCTCTTTCCTTTT | + | 7.94 | | IRF2 | MA0051.1 | chr5:150477985-150478003 | CTTCTGCTTTCTCTTTCC | - | 6.11 |
|
| | Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
| SE_00624 | chr5:150471795-150491225 | Adipose_Nuclei | | SE_09226 | chr5:150470896-150478712 | CD14 | | SE_13605 | chr5:150476429-150479236 | CD34_Primary_RO01536 | | SE_15204 | chr5:150476445-150482207 | CD4_Memory_Primary_7pool | | SE_17941 | chr5:150476396-150479537 | CD4p_CD25-_CD45ROp_Memory | | SE_18317 | chr5:150472170-150479647 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19111 | chr5:150472583-150477050 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_19111 | chr5:150477297-150478440 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_23141 | chr5:150476216-150477174 | Colon_Crypt_1 | | SE_23836 | chr5:150476528-150477056 | Colon_Crypt_2 | | SE_25002 | chr5:150476191-150477173 | Colon_Crypt_3 | | SE_25989 | chr5:150472379-150476998 | Duodenum_Smooth_Muscle | | SE_27123 | chr5:150476397-150477324 | Esophagus | | SE_28253 | chr5:150472024-150476840 | Fetal_Intestine | | SE_32472 | chr5:150476410-150478853 | GM12878 | | SE_37013 | chr5:150471038-150478454 | HSMMtube | | SE_42116 | chr5:150477374-150479546 | Lung | | SE_50074 | chr5:150472125-150478957 | Sigmoid_Colon | | SE_51316 | chr5:150479136-150480642 | Skeletal_Muscle | | SE_52353 | chr5:150472070-150481988 | Small_Intestine | | SE_53309 | chr5:150472028-150479367 | Spleen | | SE_59083 | chr5:150437761-150478457 | Ly3 | | SE_60748 | chr5:150431201-150478526 | DHL6 | | SE_62297 | chr5:150437930-150538770 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr5 | 150477506 | 150477962 | | chr5 | 150476545 | 150477196 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I151091 | chr5 | 150471363 | 150481994 |
|
Enhancer Sequence | AGCAGGCATA GTGTAGAGCA TCAGACTCCC CCCTCTGACC CTGATTACTC TTCTCTAAAA 60
TAGAATCCTG CCTATTATTG ATAATAAAGA GCTGATATAC TGAGTCCTTC GTATGTTCTA 120
GACAGTGTGC TCAGAAATAA ACATGCATTG CCAGTACAGA CAGGTCAAGT TACTTATTTA 180
CTTCTACTAA TAGTGGTGGA TGGGATTTGA ACCCAGGCCT GCCTGCCTCC ACAGACTTAA 240
CCACTGAGCA GAGGGCTCAG TTATGTAACT ACAATTTCCC ACTTGCCTCA CTCCAACCCT 300
AAAGTGGGGA AATCTGTAGG AAACCCAGGT TCTGGTGGGG AATGAAGAGG CATGTTAGAG 360
CGCTGTTTTA CCGCTTCTGG GTTCCGAAAT TCAGGTTGGG CAACCCGACC CTTCTCCCTC 420
CCATGCTCAG CTCAGTCTGG CTTCCTCATC AATAGGTAAA GGAGGAAGTG TCAGCAGAGA 480
GAGCAGAGCC TGGAATCAGG ACAGCTGCGT TCTAGCCTCA GATCTGGCAC TTACTAATAC 540
AATGGTCACA ATCCTGTCTC TGGGCCTCAG TTACCAAACC TGTGAAACGA GAGGGTTGGT 600
TGGGGCCATC TCTAAGACCA TTTCCAGTGA GTCAATCCAT GATGTACTGT CTATGTCTTC 660
AGGCAGTATG TTTCACCACT TGGAGCCCAA GTTTCCTCAT TGGTAAAAAG AGGGTGATCA 720
CCCCTATAAT ACTGCAAAGG AAGTAACGGC CATGGAGGCA AAGCTTCTCA AGTGGGATTA 780
TTCTGGTGGC GACTTATTGC TTGCAGCTGT GCTGGGGCAC CATGAATATA GGGGGATTTC 840
TTTTTTTTTT TTGAGACACA GTGTCCCTTG GTAGTCCAGG CTGGAGTGCA ATGTCACGAT 900
CATGGCTCAC TGCAACCTCC GCAACCTGGG CTCAAGCGAT CCTCCCACCT CAGCCTCTCG 960
AGACTGCAGG CATACACCAC TACCTCCAGC ATTTTTTTTT CCTATTTTTT GTAGAGACGG 1020
GGTTTTGCTA CACACAGGCT GGTCTTGAAC TGGGCTCAAG CGATCTGCCC ACTTTGGCCT 1080
CCCAAAGTGC TGGGGTTACA GGCACGGGCC ACGGCACCTG GCCATAGGGA AACTTTAAAC 1140
AGCCAGCGGT TCCCACACCA CCGCCACGGG CAGGAGGTTG AGTGGCAATT CCTAAATAGC 1200
TGCTCTCTGC TCAGGTTAAA AGGGCACCCC CCCTCCCAAT GGGCAACTTC CTTCGGGTAT 1260
TTCCTAGTGG CCCCAAAGAC CAAGATTGGC CCATCCCAGT TCAGAGCTTG TAACAGTTTG 1320
CCCTAAAGGG AAAATGCAAG GCTCAAGGCA GGAGGGGGAG CAGTGAGGAG CTAGAGAGTA 1380
TTGAAGCCCA CCTCCACAGG TGACGACAAA AGGAGAAAAC ACAGGGTGCT TCTAAAAGCA 1440
CCGGCCCTGG CCGGGATGGC AATTCCAGTT CTGTCTGCTG CTAGCTTGCT ATGTACCCTG 1500
GGCCAGTTGC TTCCTCTCTG TGGAAGTGAC AGTTGTTTCA TCTGCAAGTG AGGGAGGGAG 1560
GTGAGAATTT CTGAGGGCCC CTTCTACCCT TAGAACATCA CAGCCAGCCT CCCTTTCTCC 1620
CACTTTGAGA CAGCAGCGGT TTGGGCTTCT GCTTTCTCTT TCCTTTTAGT TTTAAATTAG 1680
CCCCCATCGC TTCTCCCGAT TAAACTTTGG CCACAGAAGC AATCTCCAGT GTCATTTTGG 1740
AGAGAGCTGA GCAGGAGGGA CACTCAGTGG AAGCTCCTTA AGCACCAGAA CCACATTGGT 1800
TTGTATGTTT TGCACCTAGC ACGTGGCATG GAACATAGGA GCCACTCATT AAGTGTAAAC 1860
TGCATGCATG CATGAATGGG GTGCTCTGGT TCAGAACAGT GGCTACTCTC CTCCTCTGCT 1920
AAAACTCCAA GAAAAAAATG TGGTTTGTTC AGCTGGCACC GAGCTCTTAG TAGGACCGTT 1980
GCAAAAGGCT CCCGAATGGC ACCCTGCCTT CCTACATTTG TCCTCAGAGC ATAGCTAGAC 2040
GCACACCTTC CCCACTCAAG AACTCCAAAG GCTTCCCCTA GGTTATCAGA GAAAATCCTG 2100
ACATTTAAAG TCCTCCTTAA TTGGAGACAA ACTGTCACTT CTCATCTTGT CTACCTCACC 2160
TCACAAACTC TTAGGGTTTC CTTCCTGCTA CCGACCAGTA CCAGAATGCA ACTACCTTAA 2220
CTGAAAATTA TGTGGAAAAT GCATGCTGAG GCATTAGGGA GGCATCAGAC AGCTACTGCC 2280
CGATTTTAGC TGTCCTCATT CCTGGTTTCT AGGCCTCCTC TTCTGTGTTC CCCTCAGCTC 2340
CATGGGCTCT CCTCACTTCT ATTCCCTGAT TCCACTCTTC TTTCCTTTCT GCCCCAAGCC 2400
CATTTCCCTC AGTATATATT TTAAGGCACT TTTCTTTTTG GGTTCAAATG CCTTTGTGAT 2460
CTGCAGCTGA CGGACTTCAT GAAATCAAAG CCATAAAGCA TCATGGGCTC CACCTTTCAG 2520
CCCCTACAAC TGAGCCTGGT TCGGGGCAGG TAGTGAGACT GACTCCGAGC CAGGCACGCA 2580
CCCTGCCAAG CACCTCCACG TGGTGCCTCC TTTTATTCCC ACAAGGCTAC AGGATAGGTG 2640
GAATTGGAAT GAGGAGCCCT GTTTTACAGA GAAGGAAACC GAAGCTCCTG TGCTGACGGT 2700
CAGTTAGTTA CAAAGGTCTT AATCCAAAAC TCTGAACCAT TTTGTTAATT TATCTTTCAG 2760
TAACAGTTCA ATTAAGTTAG ACAAATATCC CAAAAAGCTC TTAGCTGGCC CTCAAGGCAC 2820
TTGAGTTCAC AGCCCAGAAG AAAGGAAGTA AAGACACGGT AAGGTAACTT TTCTTTGTTT 2880
CAGACTCATT ATGTCAGAGA TTAAGAGAGA GCTCTTCAAA ATTGTTGGAT CCAACCCCCC 2940
ACTATAAAGT TGGAGTAACT GAGGCCCAGT GAGGGCAATG GCTGGTCTGA GGTCACAAGT 3000
GAGGGAGGGA CGAGACCAGA CTCTCTCACC TGCCTGTTGC TGTCTTCACA GCTATGAAAA 3060
CAAACACATG CGCCGCGCAC GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCAA 3120
GGCGGGTGGA TCACCTGAGA TCAGGAGTTC GAGACCAGCC TGACCAACAT GGAGAAACTC 3180
CATCTCTATT 3190
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