| Tag | Content |
|---|
EnhancerAtlas ID | HS018-20785 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr6:159270450-159272890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr6:159271832-159271847 | TTCTATTTTTGAATT | - | 6.35 | | NFAT5 | MA0606.1 | chr6:159272696-159272706 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr6:159272696-159272706 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr6:159272696-159272706 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
| SE_10307 | chr6:159270489-159272427 | CD19_Primary | | SE_11101 | chr6:159269935-159278161 | CD20 | | SE_12189 | chr6:159270476-159272674 | CD3 | | SE_14386 | chr6:159269967-159276559 | CD4_Memory_Primary_7pool | | SE_16462 | chr6:159270366-159272622 | CD4_Naive_Primary_8pool | | SE_17999 | chr6:159269964-159278117 | CD4p_CD25-_CD45ROp_Memory | | SE_18987 | chr6:159270298-159272689 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_20282 | chr6:159270258-159272560 | CD56 | | SE_20897 | chr6:159270325-159272691 | CD8_Memory_7pool | | SE_21904 | chr6:159270304-159272606 | CD8_Naive_7pool | | SE_22378 | chr6:159270210-159277819 | CD8_primiary | | SE_23109 | chr6:159270311-159272890 | Colon_Crypt_1 | | SE_23789 | chr6:159270320-159272542 | Colon_Crypt_2 | | SE_25058 | chr6:159270298-159272906 | Colon_Crypt_3 | | SE_27140 | chr6:159270275-159272234 | Esophagus | | SE_27140 | chr6:159272258-159272913 | Esophagus | | SE_27853 | chr6:159268889-159276361 | Fetal_Intestine | | SE_28795 | chr6:159268853-159276331 | Fetal_Intestine_Large | | SE_34137 | chr6:159269472-159272352 | HCC1954 | | SE_34397 | chr6:159270023-159277893 | HCT-116 | | SE_34769 | chr6:159269432-159276667 | HeLa | | SE_35994 | chr6:159268630-159276489 | HMEC | | SE_40070 | chr6:159270467-159271929 | K562 | | SE_51056 | chr6:159270265-159271835 | Sigmoid_Colon | | SE_52705 | chr6:159270267-159272097 | Small_Intestine | | SE_58403 | chr6:159210147-159292283 | Ly1 | | SE_63169 | chr6:159270185-159292330 | Tonsil | | SE_64395 | chr6:159270254-159276320 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 159270971 | 159271326 | | chr6 | 159270643 | 159272155 | | chr6 | 159271429 | 159272000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I158847 | chr6 | 159268541 | 159279766 |
|
Enhancer Sequence | AAAGAAATGG GGGAATGTGG AATCTGTCCT TGATGACTGC CACTGAATAT TCACACTAAC 60
ATCACAGTGA GGTCCCTGTT CATTTGTGCA GGAGAACATG TACAAACATT TAGGCAGAAC 120
ATACGCAGAG TAGAGTATAC AGACCTCTCC CTCCTGTTCA GGCTTTTAGC TGGCATTAGG 180
GGTTTGAGAC CTTGGAATGT TGTCAAAGAA AAACACACTT TAAAAGCCCG TTTCCAAAAG 240
GGTGACAAAC GGGACTGGAT GATGTGTTTA ACCTCATGAA ATATTGAACT CTTGGATGTA 300
AATCTGCCCA TATCACTAGA GATGAAAGAG TTATTCCTGT TTTTATGTCT AATTGTGGAA 360
CTGGTGAAAT TTGCATTTCC CTAGAATCAC TGCCCCTGTT GATAGTTGAA ACACACAGTT 420
TTGAAGAACA GCAAATCATA CTCTAAGAGG CAGTAGTCCC CTATGTCCTG TCGTTTTCCC 480
TGTTTCTGCC TTCTATAGAC ACCCTTGCCA CCACTCAGAA ATGTTTGAGA CTTTGTGGAG 540
AAAGTAGACT GGTGAGAATT TCCTCGTACT TGGAAGGGTT AAGCACTGAG TCGATCTACA 600
GCAAGTGGCA CACCCAGTTT GAGGTCCACG AGGGTGAAGT AATTTATCTG TGAGTCATAT 660
CACTGAATAC ACTGTTCTAT AGAATGTTGG TTAGCAACTC ACTTCCAAAC ATCGTGGCCA 720
ATGGTTCTGT TAGACATAAC ATTTGAAAGT GAGATGAGTT GCTCATGTGG GCTTAGCAAT 780
AGGCAATGAA ACGAATCTGG CATTGAAACA GACGTGGGTT TTTACAATGG GTTTAGACTG 840
AAAAGAAGTG CTGTGTTGCA TGAGTCCATC TTCACACTAA GCATGAAAGC CAGAGAAGGA 900
CCATCCGGTG CTCCTGGTGG AGACAGTGTC TCGGGACACT GCCTGTGAGG TTTTCAGGAT 960
AGGAAAAAGA AGAGAAAAGG AAACCCAGCC CCTTGGTTTT CTTGTTTTAT AATGTGGCCA 1020
TTTCAGAGGC TGTGACTATA GGATTAAATG CTTAGCAATT GGCAGGACTT TATATTGACT 1080
GGTGTTTAAA ACTTAAAATT CAGTTATTCC AACCACAGAT ACTATTAAAA GAACTCTGGA 1140
GTCAAGAGGA ATGAGCAGGC AAGAGGGTGA GGCTGTGTCT ATGGCTGGAG GAAAGGTGTG 1200
ATGAGTTGCT GTTTTGTTGC TAGGCAATAG GTTTTATGTG ACAACAATTC CTTTCCTTTA 1260
AAGAACTAGA GTGCTCTTTT TGTTTAATGA AAGCATTAGA TTTTCTTGGT ACAAGAGGTA 1320
CCCATTGAGT TTACGTGAAT ATGTGGTATT ATAGTAAACA GTGCTTATGA AAGGGAATGC 1380
TATTCTATTT TTGAATTCTT TTGTTTTACA TTGCCACCTC TAGAAATCAT TTGCCTGAGG 1440
AGATGTGGTT TTTTCCTTTT CTCAAATGAT TTCTGTTGTT TGGCTTGTCT GACTGTAAAC 1500
CTCTAAATTA CCCCCAGCTG TTATGAATGT GCTTCTGAAT TTCTCAACAG ATAGCATAGC 1560
ATGTTTGTGT TTGGGGATGT TAGAAGATTT GCTTTTATAA TTCCAAACTA GTTAACAAAT 1620
CCTGATGTAA ATATGTTATG GTATCTTCTA TATTTCTTCT TTTATTGATC CTATTATAAT 1680
GTAAAATGTT GTAGACTGCT TATGGTCACA TTAAGACAGG GCCATATATC TCTTGCATCC 1740
TTATAGCCTT AATACCAATC TAACATAAAA CTTGGCATAT AGTTTATATC AATAAATGAA 1800
CGGTTGTTGA ATAAGTGAAT GAATGGATGC ACAAATCATT GATATACTGT TGCATTTTCC 1860
AGTGACGTGG ATTTATTTAT TTATTTATTT ATTTATTATT TTGTTTTTGA GATGGAGTCT 1920
CGCTCAGTCT CCCAGGCTGG AGGGTAGTAG TACGATCTCA GCTTACAGCA ACCTCTGCCT 1980
CCCCTGCCTC TCCGGTTCAA GCGATTCTCC TGCCTCAGCC TCCTGAGTAG CTGGTATTAC 2040
AGGCATCTGC CACCATGCCC TGCTAATTTT TGTATTTTTA GTAGAAGATG AGGTTTCACC 2100
ATGTTGGCCA GGCTGATGTA AAACTCCTGA CCTCAAGTGA TTCACCTGCC TCGGCCTCCC 2160
CAAGTGCTGG GATTACAGGC GTGAGCCACT GCGCCTGGCC TGATAATATT CTTCTATATT 2220
TTAGAGACCA TGGAGTTAAT TCTAAAAATG GAAAATACTT AGGCCTGAAT ACCAGCCCAT 2280
AGGTTTACTA TTTTTCCCTA AGGTAATGTC TTCTCCTTAA GCAGCATTAG AGCTTTGCTA 2340
ACATGCCATC TAAAAATGTA CCCCCCAAGC TGGGCTCAGT GGCTCACGCC TGTAATCCCA 2400
GCACTTTGGG AGGCCGAGGC AGGCAGATCA CCTGAGGTTG 2440
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