| Tag | Content |
|---|
EnhancerAtlas ID | HS040-31006 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr6:159273360-159276270 |
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 | CTCACAACTA CACTATGAAG CGGATGCTAC TATTGTCCAC TTTATGGGGG AAGAAACTGA 60
GGCACAGAGA GGTTAGCTTG CCTCGGGACT CTGTCTCTGC TGAGATTGGA AGCAGAAGAC 120
TAGTTCCAGA ATTCACACTC CTAACCCTAC TACAACACCT GCTCTCAAAC AGAGAAGGGA 180
AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG ATCTTGTGCT GGTCTGGTCT GGACATGGAC 240
CAAGGCTTGG GGGCCTTGCA CACGTAAGTG AGTGCAGATG CCCGGCCCAG CCCCAGGGCT 300
CCCTTGTCCT TGAGCTGGGG CCACGCTGAG GCTGAGGCTG GCCTCCATGG CTTGACTTGA 360
GGCCACCTCC AGATCCACAC CCTGAAAGCT TGGGACTGGC CTTCTCAGAG AATGGGGCAA 420
AACACTCTGA CGCCAACTAC AACCATCACA AGGAGGTACA TTCTCTGTAA GGGCAAGCCT 480
GGGGCTGCAC CCAAGTAGAC TAGCAGACAC TCATTACAGA GAGAATGTTC TGGCACTCTG 540
GCCCTGCCAA AGGCTACCAG AACACAGAAG GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG 600
CAGGCACACA CCATATGCCT CACTCACCAC ACGAAACCAC ACACCACATA GCACACACGC 660
GTGCACCCTC ATACCACACT GACCCTTCAC CACACACACA CCCATACACC TTCATGTCAC 720
ACATACCACA CACACAGATA TACCACATGC ACCCCATACA CCCCACCACA CACATACAAA 780
CACCACACCA TATACACACA CACACAGTAC AACATACACA CTCACACACC ATATGCCACA 840
CACATATACT TTACACATAT ACATACCTCC AAACACACAC CATGCACACA CACGGTACAC 900
CATACACACA CCACACACTA TGCACACACC ATGTACCACA CACATACCCC TCCAACATCA 960
CATGAACACT ACGCACCCTC CCCCATACCA CACACATACA CGCACACGTA CCATGCACGC 1020
ACACACACCA CAATGTGCTG TTACTTAACA GGTTTGCCTT CCCACAACTC TATCAGCAAA 1080
CCCTTCTGGA GGCGCAGCCC ACACCTGCAT TCCAAAGAAC GCAAATCCCT TCCCTGCCCG 1140
ATGAAAGGCC CCTCCCACAG TGAGTCACAG AAACTGCAGC CGAGCAGGCA GTGGTGGGCC 1200
CCACCCTTCT CACAGGAAGT GAGAAAGAGT AAATATGTAG TTTTTCTTTG AGGGCCAATG 1260
CACATGTTAA ATGGGTGATT AAGAAGACAG AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA 1320
CAATGTCTGG GGACTTGGCA GTAGCCTGGC AGAGACCGCA GGAATCCTAT AGAGTCTTTT 1380
ATGGACAGGG CTCTGAAATT CCAGAGCCTG CAGGAGGTAC CTTCCCCTTT GACTCGGCGG 1440
GGCTGTACCA CTAAGAATGC ACTGAGCATT GGGTGCACTT GGGATACCTG AGCTGTGGGG 1500
CCAGAGAGGC AGCCCTAGGG GAGAATTCCG GAGTTGGGGC TGGGTTCTTT CAGCATAAAA 1560
AATCAAAGTG TCGCTTCTTT AATGAACCTC CCGGCAAGGT CTTCCCTGAA GACCTTGAAC 1620
AAGTGTTCTT AAACAAGTGT TCCTTTATGC AATTAAAGGC CAGGGAAGCT GGGGTCTGAG 1680
AGGCCATGGA GCCATTGGGA TAATAGTGAC AGTTCGGCTA CCATTCAACT GGGCTTCTGA 1740
TGAATCATGC TGGGGGCAAG GACTCCAAAT CACCAGCTCT ACTCTATACT CGAATCAGTA 1800
GGCAGTTCAG ACAGTCTTGG GGGATTTGGG CAAACGAACG CTCCACTTAG AATCTCTCCA 1860
GAAAGACAAA GGGGGTGCCT AACAAACAAT TCAAGGACTG TGGGAAACCA ATGATCATCA 1920
AGGGCTCAGT TGTACAGTGT AAACCAAAAA GTATCTGAGA CAGGTCTCAA TCAACTGAGA 1980
AGTTTATTTT GCCAAGGTTA AGGACAGGCC AGGGAGGAAG AAACACGGAA TCACAGAAAC 2040
AGTCTATGGT CTGTGTCGTT CTTCCAAGAT GATGTTGAGG GCCTCGATGT TTAAAAGGGA 2100
AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC ATGGGAATCT ACTTGTTGCA AGGGAAAAGG 2160
AGCAGGAAGA GGAACAATCA GTTACGTTTC CTCTAGCAGT CTGTAAATTG GTGCTTTACA 2220
TAAGATGAGC ATAGAGTTTA GCTGCCTGTG GTGGGGATAT CTAGCCTTTT ATCTGTAGCT 2280
ATCTGCTTAG GCACAAACAG AAAGGCAGCT TCTTGCATGA CTCAGCTTCT AGTTTAATTT 2340
TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC TGAGAGTTTT TCTTTTCCTT TCACAACAGG 2400
AAGAAACAAA CTACAGAGCC CCTAGGTATA CTGGGGCCAC CTGGGGTCTT GTTAAAAATG 2460
TGCATTTGGG GGAGGGGCGG AGAGTCTGCG TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT 2520
CTGTAGGCCA CACTTTGAAT ACTGAGAGTA CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG 2580
GGTGGATTCT GGTACAGTTG GAGGGAGGAG GCTTCCTGGG GTGAGGGCAC TGAGATGGGT 2640
CCTGGTGGTA AGATTGTGTG GGGAGGAGAA TAAAGGTACC CCAGATCAAC CTTGTGGGGC 2700
AACAAGTGAC CTGACAAACT CCCATCATGT ATGGCCACTG TCCCCCATTC AAGGCCAGGG 2760
ACCGTTGGAG GAGTTGGAAA GTTAAGAGCT TGAAAACTGG ATTCTGCCTC ACTGGGAGGT 2820
TCACTGACAT TTAGTCTTCT CTGAAAGATG GGCATAGTTA TACCAATCCT ACAGGAGTAG 2880
TGTGAAGATT AAATGAGATG ACATATAAAG 2910
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