| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00050 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:26614640-26617060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata1 | MA0035.3 | chr1:26615310-26615321 | ACAGATAAGGA | - | 6.14 | | NR2C2 | MA0504.1 | chr1:26615100-26615115 | TAAGGTCAGAGGGCA | + | 6.36 |
|
| | Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
| SE_09234 | chr1:26600437-26620418 | CD14 | | SE_10276 | chr1:26609716-26620076 | CD19_Primary | | SE_11598 | chr1:26601677-26620618 | CD20 | | SE_12127 | chr1:26609517-26619068 | CD3 | | SE_13098 | chr1:26613251-26615233 | CD34_Primary_RO01480 | | SE_13098 | chr1:26616441-26617910 | CD34_Primary_RO01480 | | SE_14176 | chr1:26610126-26617625 | CD34_Primary_RO01549 | | SE_15660 | chr1:26609807-26618647 | CD4_Memory_Primary_8pool | | SE_16821 | chr1:26610331-26617967 | CD4_Naive_Primary_8pool | | SE_17222 | chr1:26613332-26618016 | CD4p_CD225int_CD127p_Tmem | | SE_17706 | chr1:26601754-26619073 | CD4p_CD25-_CD45RAp_Naive | | SE_18032 | chr1:26601635-26619607 | CD4p_CD25-_CD45ROp_Memory | | SE_18600 | chr1:26600628-26620343 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19301 | chr1:26601729-26619077 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_20500 | chr1:26609324-26619072 | CD56 | | SE_21239 | chr1:26609862-26619058 | CD8_Memory_7pool | | SE_22719 | chr1:26601924-26619047 | CD8_primiary | | SE_23529 | chr1:26614798-26615598 | Colon_Crypt_1 | | SE_24040 | chr1:26614643-26615249 | Colon_Crypt_2 | | SE_24040 | chr1:26615778-26617811 | Colon_Crypt_2 | | SE_26906 | chr1:26613419-26617713 | Esophagus | | SE_31060 | chr1:26610152-26618849 | Fetal_Thymus | | SE_31862 | chr1:26614480-26617883 | Gastric | | SE_40404 | chr1:26609226-26616392 | K562 | | SE_41449 | chr1:26613365-26617866 | Left_Ventricle | | SE_42616 | chr1:26613355-26618804 | Lung | | SE_50183 | chr1:26601943-26618863 | Sigmoid_Colon | | SE_52659 | chr1:26613372-26618804 | Small_Intestine | | SE_53610 | chr1:26609706-26619005 | Spleen | | SE_55161 | chr1:26613407-26618780 | Thymus | | SE_62762 | chr1:26609498-26620090 | Tonsil |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr1 | 26616270 | 26616483 | | chr1 | 26616527 | 26617019 | | chr1 | 26615527 | 26615997 | | chr1 | 26615016 | 26615421 |
|
Enhancer Sequence | GCCCAGAAAG GTCAGATGAC ATGGCCTGAT CAGACCAGAC AGAGCCAGGA AGAGCACCAA 60
ATACACCAAC TCCTAATTCA ATGCTCCTGC CGCCTCCCAG GGCCGGGGGT TTTTCAGGCT 120
GATGAACATG GGTGGTTGAC ATGGGATGGG GTGAGACCAG GGAGGATGCC AAGAAACGAC 180
GAAGGGGAAG AGAGAAGCTT GCCAAGAAAA TGGCCCTGGC TTAAAGAAGT AAAAGCAGGT 240
GGCCCAGGCA GATGCTGGAT ATGATAGAGT GGAGATGAGA CCAGGGGCCA GGAAGAAGGA 300
ACCACAGCTC TGGGCAAACC AGCACTGAGA GAATGAGGTG GGAAGAGCTA CCACAGCAGG 360
GCCTTGTGAA GCCAGTGAGC CCCCACCACC CCACCAGGGT TCAACTGAGG CCTGACCCGT 420
GGATGGAGAG AGGTGCAGCT GGGGAGTCAC ACAGCAGGAG TAAGGTCAGA GGGCAAGTCC 480
TAGGTCTGCC CTGAGCTAGC AGCAGAACTC AAATGGAAAG GCACTTCCTC TTTGAGCCAC 540
AGCCATCCTT TCTGTGCAAT GGGGAGATGG TAAGAACCCT GTACTGCCTG CAAGATCCAG 600
CTGGTGAACC TGTCTGTAAA TGACAGCCCT GTGCCAAGCG CCAGGAGGCA GGCATCACCA 660
TTTCTGTTTT ACAGATAAGG AAATTGGGCC TTATGAGCTG TCACGCCCCA GATCATGCAG 720
CTTGCAGGGC CCAAGTGACT CAGCCTCAGT GCTCAGTGAT CACATAGGCT GCCTCTCAAT 780
ATTGGTTCTT GAGAGGCTGC TTACTGGGGT CCCTTTTCCA GGGAGAGTGG CAATGCTGGG 840
AGATCACCTC TGAGGCCTCA TCCAACTTTG AGAGCCCACG AGTGTATTAA AATGAGAAGG 900
GAGCTCAAGT CCAAGCTCTT TGTCCCAACT CCCAAGACCC TTACTTAGCA CCCAGCCAAC 960
CCTCAACATG CCCCTCGCCT TGCGCTCTGG TGGGCACTGG AGGGCACTTC CGAGCTCTGT 1020
AACCCTGGGC CTCTATGGGC CTCAGCTTCC TCTTCTGTAC AATGAGGACG ATAAAAGTTT 1080
CCACACTTCA CAGGGCTGCT GTGAGGCTTG GAGGAAGCGT TTGGCAGATG GTGGCTGTTG 1140
TTGTCCCTAG CACCGCCTAC TCATCGCTGG GCTCAAGCTG TGCCCACTCA CCCCTACCTC 1200
CTCCAAGAAG CCTTGCTAGG AGCCACCCCC AACCTGCCTT GAGGCTGCAT GCCTGGAGCC 1260
CTTGCACCTA CTCCCTTGGC CCTCGTCACA GGCCGCTGCT TTCTGCTTGC TTGTTTGCCT 1320
TCCAGCCATG CTGGGCACCC CTTGAGCTCA GGAGCATTGA GCCCTGGGCC TGGCCCAGAG 1380
TGGCTGGGCC ACTAAAAGCA GGGTTGGATC CTGCTTTCCA GAAATGTCTG AGCACCCGTG 1440
CTCTGCTAGG CCCTGCCCAT CATGGCGATG CCCACGCCCA GGGTCCTGCC ATCCTCAGGC 1500
TCAGACTCAA GTGAAGAAGA CGGGGCGGCA AATGGCGACA ATGGCATGTG TAAGTATCAC 1560
TGTGGGGGCT GTGGAGCCCA GAAGAGGGCC AGACCCTACC ATGCTCAGTG GAGAGGTGGC 1620
AGCCCCTCAC TGCACAAGTG CCCAGGGCAC CCCGGCAGCT CACGCGGTGC CGCCCTCCAT 1680
GTGCCTGCCC TTGACCCTCA GGCAAAGACG GCTGCAACAG GAAGTGGAAC CACTATTACC 1740
ACACACCTGC AAGCCAGGCC CCGCTCTGGG GACTTTACTG CAGTCACTCT GCTCTTCAGA 1800
GGAGCCAGTG CAGGAAAGGA GGCCCTGCAG GTCTGGTCCC CGCCAGAACA CTCAACCAGC 1860
CTGTGGACTG GCAGGATCTG AACTCAGGCC TGCCGGGTCC CACCTGCAGC TCTCTCTGGC 1920
CCCTGCCATT GAGCTACGCA CCACCCTGTC CCCACCTCAT CATGTGCAGA TGACTGTTCC 1980
AATGTGCTCT GATCATCCAA GCCTGGGCAC ACGGGCATCA CAGCCAATCA CATGCAGCTA 2040
CACACACCCT TGCCCATGTG CCAAGCACTG GGACATGCAT GACAACAGCT AGGTGACAGT 2100
GGCTGTCACA GTTTATTACC ACATCCATTC AGTGGCCCTA GGAGCCCGTC AGCACGACTG 2160
AGGAGGAAAT GAACTCAGAG GGGGTCAGCG ATCTGCTGAT CTGGGGTCTG ACCCGACCTG 2220
AACCCTGCCT CAGCCAGAGC TTTTAGCCCC TTCCCTCAAG CAGAGCCCTC CCCACAGAGC 2280
AGCACAGCCC ACACAGGGCA GTCAGAGTTT GCTGGCGGAG GTTGGATTTG CCCTGAGCTT 2340
CAGAGGGGAG GGAAGCGGGC AAGGCGCTCT GTGGGGACAG AGCAGGAGCA AAGGCTGGAG 2400
GCAGAAGTGC AGGTGGGGAG 2420
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