| Tag | Content |
|---|
EnhancerAtlas ID | HS052-34120 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr6:159273420-159276000 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr6:159274110-159274130 | ACCCCATACACCCCACCACA | + | 6.14 | | RREB1 | MA0073.1 | chr6:159275925-159275945 | TGGTAGGGGGTGGTGGGTGG | - | 7.57 | | TCF3 | MA0522.2 | chr6:159273513-159273523 | AACACCTGCT | + | 6.02 |
|
| | Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
| SE_10307 | chr6:159273179-159276502 | CD19_Primary | | SE_11101 | chr6:159269935-159278161 | CD20 | | SE_12189 | chr6:159273267-159276491 | CD3 | | SE_14386 | chr6:159269967-159276559 | CD4_Memory_Primary_7pool | | SE_16462 | chr6:159273351-159276594 | CD4_Naive_Primary_8pool | | SE_17999 | chr6:159269964-159278117 | CD4p_CD25-_CD45ROp_Memory | | SE_18987 | chr6:159273136-159277721 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20282 | chr6:159273082-159276574 | CD56 | | SE_20897 | chr6:159272786-159276642 | CD8_Memory_7pool | | SE_21904 | chr6:159273108-159276540 | CD8_Naive_7pool | | SE_22378 | chr6:159270210-159277819 | CD8_primiary | | SE_23109 | chr6:159273079-159276256 | Colon_Crypt_1 | | SE_23789 | chr6:159273267-159275641 | Colon_Crypt_2 | | SE_23789 | chr6:159275700-159276183 | Colon_Crypt_2 | | SE_25058 | chr6:159273048-159276283 | Colon_Crypt_3 | | SE_27140 | chr6:159273240-159276220 | Esophagus | | SE_27853 | chr6:159268889-159276361 | Fetal_Intestine | | SE_28795 | chr6:159268853-159276331 | Fetal_Intestine_Large | | SE_34137 | chr6:159273141-159276469 | HCC1954 | | SE_34397 | chr6:159270023-159277893 | HCT-116 | | SE_34769 | chr6:159269432-159276667 | HeLa | | SE_35994 | chr6:159268630-159276489 | HMEC | | SE_40070 | chr6:159273143-159276574 | K562 | | SE_51056 | chr6:159273219-159276293 | Sigmoid_Colon | | SE_52705 | chr6:159273298-159276322 | Small_Intestine | | SE_58403 | chr6:159210147-159292283 | Ly1 | | SE_63169 | chr6:159270185-159292330 | Tonsil | | SE_64395 | chr6:159270254-159276320 | NHEK | | SE_69169 | chr6:159273396-159276424 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I158847 | chr6 | 159268541 | 159279766 |
|
Enhancer Sequence | GGCACAGAGA GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA AGCAGAAGAC 60
TAGTTCCAGA ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC AGAGAAGGGA 120
AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT GGACATGGAC 180
CAAGGCTTGG GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT 240
CCCTTGTCCT TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA 300
GGCCACCTCC AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA 360
AACACTCTGA CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT 420
GGGGCTGCAC CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG 480
GCCCTGCCAA AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG 540
CAGGCACACA CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC 600
GTGCACCCTC ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC 660
ACATACCACA CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA 720
CACCACACCA TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA 780
CACATATACT TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC 840
CATACACACA CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA 900
CATGAACACT ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC 960
ACACACACCA CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA 1020
CCCTTCTGGA GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG 1080
ATGAAAGGCC CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC 1140
CCACCCTTCT CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG 1200
CACATGTTAA ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA 1260
CAATGTCTGG GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT 1320
ATGGACAGGG CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG 1380
GGCTGTACCA CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG 1440
CCAGAGAGGC AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA 1500
AATCAAAGTG TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC 1560
AAGTGTTCTT AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG 1620
AGGCCATGGA GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA 1680
TGAATCATGC TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA 1740
GGCAGTTCAG ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA 1800
GAAAGACAAA GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA 1860
AGGGCTCAGT TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA 1920
AGTTTATTTT GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC 1980
AGTCTATGGT CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA 2040
AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG 2100
AGCAGGAAGA GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA 2160
TAAGATGAGC ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT 2220
ATCTGCTTAG GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT 2280
TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG 2340
AAGAAACAAA CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG 2400
TGCATTTGGG GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT 2460
CTGTAGGCCA CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG 2520
GGTGGATTCT GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT 2580
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