| Tag | Content |
|---|
EnhancerAtlas ID | HS129-32699 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:159273210-159276190 |
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 | GTCTCTCAGG TTTTGGAGAA TTAAAATGCC TCCCTTATCC CATCCCTGCC ACACTCTAGG 60
ACATTGATTC ATGTTCCCAA AGAATAATGG TTAGCTTACT GTATGCCAGC TACTATTCTT 120
AGCTCCTTAC ATGAACTAAT CCTTTTAATC CTCACAACTA CACTATGAAG CGGATGCTAC 180
TATTGTCCAC TTTATGGGGG AAGAAACTGA GGCACAGAGA GGTTAGCTTG CCTCGGGACT 240
CTGTCTCTGC TGAGATTGGA AGCAGAAGAC TAGTTCCAGA ATTCACACTC CTAACCCTAC 300
TACAACACCT GCTCTCAAAC AGAGAAGGGA AAGGAAGTCC TGGCGTTTGC ACTCTCCTTG 360
ATCTTGTGCT GGTCTGGTCT GGACATGGAC CAAGGCTTGG GGGCCTTGCA CACGTAAGTG 420
AGTGCAGATG CCCGGCCCAG CCCCAGGGCT CCCTTGTCCT TGAGCTGGGG CCACGCTGAG 480
GCTGAGGCTG GCCTCCATGG CTTGACTTGA GGCCACCTCC AGATCCACAC CCTGAAAGCT 540
TGGGACTGGC CTTCTCAGAG AATGGGGCAA AACACTCTGA CGCCAACTAC AACCATCACA 600
AGGAGGTACA TTCTCTGTAA GGGCAAGCCT GGGGCTGCAC CCAAGTAGAC TAGCAGACAC 660
TCATTACAGA GAGAATGTTC TGGCACTCTG GCCCTGCCAA AGGCTACCAG AACACAGAAG 720
GCCCTTTCTT CCAAGGGGCC GAAGGAGGAG CAGGCACACA CCATATGCCT CACTCACCAC 780
ACGAAACCAC ACACCACATA GCACACACGC GTGCACCCTC ATACCACACT GACCCTTCAC 840
CACACACACA CCCATACACC TTCATGTCAC ACATACCACA CACACAGATA TACCACATGC 900
ACCCCATACA CCCCACCACA CACATACAAA CACCACACCA TATACACACA CACACAGTAC 960
AACATACACA CTCACACACC ATATGCCACA CACATATACT TTACACATAT ACATACCTCC 1020
AAACACACAC CATGCACACA CACGGTACAC CATACACACA CCACACACTA TGCACACACC 1080
ATGTACCACA CACATACCCC TCCAACATCA CATGAACACT ACGCACCCTC CCCCATACCA 1140
CACACATACA CGCACACGTA CCATGCACGC ACACACACCA CAATGTGCTG TTACTTAACA 1200
GGTTTGCCTT CCCACAACTC TATCAGCAAA CCCTTCTGGA GGCGCAGCCC ACACCTGCAT 1260
TCCAAAGAAC GCAAATCCCT TCCCTGCCCG ATGAAAGGCC CCTCCCACAG TGAGTCACAG 1320
AAACTGCAGC CGAGCAGGCA GTGGTGGGCC CCACCCTTCT CACAGGAAGT GAGAAAGAGT 1380
AAATATGTAG TTTTTCTTTG AGGGCCAATG CACATGTTAA ATGGGTGATT AAGAAGACAG 1440
AGAGCTGCTT AAAAGGTCAT GGGAGAAGTA CAATGTCTGG GGACTTGGCA GTAGCCTGGC 1500
AGAGACCGCA GGAATCCTAT AGAGTCTTTT ATGGACAGGG CTCTGAAATT CCAGAGCCTG 1560
CAGGAGGTAC CTTCCCCTTT GACTCGGCGG GGCTGTACCA CTAAGAATGC ACTGAGCATT 1620
GGGTGCACTT GGGATACCTG AGCTGTGGGG CCAGAGAGGC AGCCCTAGGG GAGAATTCCG 1680
GAGTTGGGGC TGGGTTCTTT CAGCATAAAA AATCAAAGTG TCGCTTCTTT AATGAACCTC 1740
CCGGCAAGGT CTTCCCTGAA GACCTTGAAC AAGTGTTCTT AAACAAGTGT TCCTTTATGC 1800
AATTAAAGGC CAGGGAAGCT GGGGTCTGAG AGGCCATGGA GCCATTGGGA TAATAGTGAC 1860
AGTTCGGCTA CCATTCAACT GGGCTTCTGA TGAATCATGC TGGGGGCAAG GACTCCAAAT 1920
CACCAGCTCT ACTCTATACT CGAATCAGTA GGCAGTTCAG ACAGTCTTGG GGGATTTGGG 1980
CAAACGAACG CTCCACTTAG AATCTCTCCA GAAAGACAAA GGGGGTGCCT AACAAACAAT 2040
TCAAGGACTG TGGGAAACCA ATGATCATCA AGGGCTCAGT TGTACAGTGT AAACCAAAAA 2100
GTATCTGAGA CAGGTCTCAA TCAACTGAGA AGTTTATTTT GCCAAGGTTA AGGACAGGCC 2160
AGGGAGGAAG AAACACGGAA TCACAGAAAC AGTCTATGGT CTGTGTCGTT CTTCCAAGAT 2220
GATGTTGAGG GCCTCGATGT TTAAAAGGGA AAAGTGGGCT GGAGAGGAAA GAGGAAGGGC 2280
ATGGGAATCT ACTTGTTGCA AGGGAAAAGG AGCAGGAAGA GGAACAATCA GTTACGTTTC 2340
CTCTAGCAGT CTGTAAATTG GTGCTTTACA TAAGATGAGC ATAGAGTTTA GCTGCCTGTG 2400
GTGGGGATAT CTAGCCTTTT ATCTGTAGCT ATCTGCTTAG GCACAAACAG AAAGGCAGCT 2460
TCTTGCATGA CTCAGCTTCT AGTTTAATTT TTTCCTGTTG CCAAGAAAAA ACTGGGGTCC 2520
TGAGAGTTTT TCTTTTCCTT TCACAACAGG AAGAAACAAA CTACAGAGCC CCTAGGTATA 2580
CTGGGGCCAC CTGGGGTCTT GTTAAAAATG TGCATTTGGG GGAGGGGCGG AGAGTCTGCG 2640
TTCCCCCCAT GCAGTGCCCA GGCTGCTGCT CTGTAGGCCA CACTTTGAAT ACTGAGAGTA 2700
CCAGAGAGGA CTTGGTGGTA GGGGGTGGTG GGTGGATTCT GGTACAGTTG GAGGGAGGAG 2760
GCTTCCTGGG GTGAGGGCAC TGAGATGGGT CCTGGTGGTA AGATTGTGTG GGGAGGAGAA 2820
TAAAGGTACC CCAGATCAAC CTTGTGGGGC AACAAGTGAC CTGACAAACT CCCATCATGT 2880
ATGGCCACTG TCCCCCATTC AAGGCCAGGG ACCGTTGGAG GAGTTGGAAA GTTAAGAGCT 2940
TGAAAACTGG ATTCTGCCTC ACTGGGAGGT TCACTGACAT 2980
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