Tag | Content |
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EnhancerAtlas ID | HS056-13031 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr6:3355700-3357430 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr6:3356284-3356305 | GGAGGGGGAGGAGGCGGGGGG | + | 6.04 | ZNF263 | MA0528.1 | chr6:3356300-3356321 | GGGGGCGCGGGAGGGGGAGGA | + | 6.21 | ZNF263 | MA0528.1 | chr6:3356325-3356346 | GGAGGAGGCGGGGGTGGGTGG | + | 6.72 | ZNF263 | MA0528.1 | chr6:3356312-3356333 | GGGGGAGGAGGCGGGAGGAGG | + | 6.88 |
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| Number of super-enhancer constituents: 28 | ID | Coordinate | Tissue/cell |
SE_00561 | chr6:3353437-3359773 | Adipose_Nuclei | SE_03267 | chr6:3354759-3356322 | Brain_Angular_Gyrus | SE_03267 | chr6:3356335-3358651 | Brain_Angular_Gyrus | SE_03899 | chr6:3348711-3360207 | Brain_Anterior_Caudate | SE_04816 | chr6:3348588-3362340 | Brain_Cingulate_Gyrus | SE_05855 | chr6:3348393-3365672 | Brain_Hippocampus_Middle | SE_06865 | chr6:3350193-3360135 | Brain_Hippocampus_Middle_150 | SE_07816 | chr6:3348168-3361219 | Brain_Inferior_Temporal_Lobe | SE_23195 | chr6:3355507-3356327 | Colon_Crypt_1 | SE_23195 | chr6:3356333-3357767 | Colon_Crypt_1 | SE_23990 | chr6:3355508-3356186 | Colon_Crypt_2 | SE_23990 | chr6:3356347-3357547 | Colon_Crypt_2 | SE_26116 | chr6:3354641-3358711 | Duodenum_Smooth_Muscle | SE_26690 | chr6:3354592-3356328 | Esophagus | SE_26690 | chr6:3356345-3357499 | Esophagus | SE_27773 | chr6:3355170-3357717 | Fetal_Intestine | SE_28645 | chr6:3355119-3358068 | Fetal_Intestine_Large | SE_31490 | chr6:3354918-3357558 | Gastric | SE_40507 | chr6:3353895-3357170 | K562 | SE_42040 | chr6:3355730-3356255 | LNCaP | SE_42040 | chr6:3356341-3357263 | LNCaP | SE_47955 | chr6:3355632-3356284 | Pancreas | SE_47955 | chr6:3356353-3357352 | Pancreas | SE_50390 | chr6:3354191-3356309 | Sigmoid_Colon | SE_50390 | chr6:3356335-3358639 | Sigmoid_Colon | SE_52843 | chr6:3354403-3356324 | Small_Intestine | SE_52843 | chr6:3356335-3358567 | Small_Intestine | SE_63339 | chr6:3333619-3356971 | NCI-H82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 3357200 | 3357407 | chr6 | 3356337 | 3357200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I003353 | chr6 | 3354095 | 3358923 |
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Enhancer Sequence | AATATAAATG TATTTATAGA TAGATATTTT CCCTCTTACC ATGTGTATAA GAGAACAGGA 60 CGTTGCTGGG CAGAGGGAAG TTATTGTGTG AAGGCCAAGG TCATAACAAG GTTACCGTTC 120 TCATGAGTCT GGGCTAGGTC TGGGCCCTCC CGCCCCGCTC CCTGTATCAG CCCCACTCCC 180 AGGCTCCAGA GCTAGGCCAC TTGATGCCTG GTCAGTCCTT TCTGTGCCTT CCCAAATTTA 240 CTCTCAATTT CTGGCTCATC TACTATTCTC ATTTGCTATT TCTTAAGTTC TGGGCCACGG 300 GAGCCCAAGG TCTCACTCAG CCCTGCACAA ACCCCAGCTC TCAAAGCCGG CGTCGCTCTC 360 ACTCATTCCC TGTCTCCGCA TCGACACGGA GGAGCCACTG GATATAACGC TGAGGTATTA 420 AAAAAAGAAG GAAGTTCAGA AAAACAAACA CAGTACGACA GCATTTGTAG GAAGTTTTTT 480 TTTAAAGGCA AAACTGTACA ACGCAGTGTT CTAGATGTGG GAAAACCTAA CGAAACTCAT 540 GAGGATGAAA AACAGCAAAC GGGGTGGGGA GACTTGTGGA CAGGGGAGGG GGAGGAGGCG 600 GGGGGCGCGG GAGGGGGAGG AGGCGGGAGG AGGCGGGGGT GGGTGGAGGC GGGAGGGTGG 660 GACTTATTAA TGAGGCTTGT TTCCGAGTCC GGGTAGCAGA TACACGTGAC ATCAGAAACA 720 TCTCATAATC ACGAAAGAAA TCGAAGCACG CGTGCTCTCT CGGGAGGGCC CTCCTTCTGC 780 GTGCCAGCCC TTGGGATCTG GACTTCTGGC TCCTGGAAAC ATTCAAAAGG AAACCGGTGG 840 GCCATGGAAC CGCTGACAGG ATTGGATGGT AAAACAGTGT CTTAGATCCA CCCTCGGTGC 900 CTACAAGGGT AACAGGCCAC ACCCCCATCT CAGAGATGGC AGCGACCTCA TCCAAGGGGC 960 AGGGGAAGCC TCAGAGGAGT GATTTTAGCA GCCTCTCACT TCCTCATTTG CCTGTGAAAA 1020 TAAAGCTGAC CCTAAACTTA CCGGCTCTGC ACTACCCTCC CGCTGGCTGC TTCATTGTCC 1080 TGGGCAAATC TTCAGCCCCA GAGACAGTAG TGTTTATTTT AGAACCAAAC CCGCTGGCCA 1140 GGACACCATC CACGTGAAAC ATTTCTTCCT AAGCCTGAAG CTTTGTTGTA ACCCTGTTGT 1200 CTTCCTCCTT ATTGGCTCAG CAGTGAGATG GGCTGGCTTG AACCTCCAGG TCTTGAAACC 1260 TGCCCAAGAT ACCAACAACC ACCTGTAATA AGGTGCAGGA TCCCGCTCAA GCCCTTCAGA 1320 GCATCTGTGG ATGTGTTACC TCATATGCCC TCACCAAATC CTATAAATAA GAATATCAAG 1380 TAGTATCCCC ATTTCCAAGA TGGGAAATGG CCCCTTCAAA GGTCAGGTCA CCGACACTGT 1440 GATGCAGGTG GTGTCTCTAG GAGAGGCGCA GGCTTCTAGA TCCCAACTGT CGTGGTTTGT 1500 TCTAAAGGCT GCAGCAGCCT GGACCATAAA GACAATTTTA AAGCAGTAAA CCTAGCAATA 1560 CAGCCTGGAA GAGAAAACCA AAACAGAGCC AAAAAAAAAA AAAAAAAAAA AAAAAAAACC 1620 CAAAACAAGG CAGGCACTGT AATGAAATGC TCACATTTAC TCCAGTGCCC ACATCTGCAT 1680 TCCCAGAGTC TCAGAAATCC AGCAGGATTC CAATGCCATG GAAATATGTA 1730
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