EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS019-08429 
Organism
Homo sapiens 
Tissue/cell
CD20+ 
Coordinate
chr19:39125760-39127040 
Target genes
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
TBX21MA0690.1chr19:39126888-39126898AAGGTGTGAA+6.02
TBX2MA0688.1chr19:39126888-39126899AAGGTGTGAAT+6.02
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00117chr19:39126719-39127932Adipose_Nuclei
SE_03166chr19:39125423-39125932Brain_Angular_Gyrus
SE_03903chr19:39125172-39126135Brain_Anterior_Caudate
SE_06803chr19:39125081-39126309Brain_Hippocampus_Middle_150
SE_07777chr19:39124999-39128150Brain_Inferior_Temporal_Lobe
SE_14624chr19:39125409-39128000CD4_Memory_Primary_7pool
SE_19537chr19:39126410-39128305CD4p_CD25-_Il17p_PMAstim_Th17
SE_20249chr19:39125184-39128305CD56
SE_22709chr19:39125315-39128147CD8_primiary
SE_23062chr19:39125394-39125979Colon_Crypt_1
SE_23062chr19:39126303-39128540Colon_Crypt_1
SE_23732chr19:39126383-39127068Colon_Crypt_2
SE_24739chr19:39125322-39126070Colon_Crypt_3
SE_24739chr19:39126271-39128151Colon_Crypt_3
SE_25779chr19:39126515-39128552Duodenum_Smooth_Muscle
SE_26525chr19:39125324-39126266Esophagus
SE_26525chr19:39126294-39128542Esophagus
SE_27614chr19:39126129-39128564Fetal_Intestine
SE_28533chr19:39125197-39128591Fetal_Intestine_Large
SE_31384chr19:39125353-39125941Gastric
SE_31384chr19:39126254-39128532Gastric
SE_34299chr19:39125367-39126196HCT-116
SE_34299chr19:39126353-39127223HCT-116
SE_34681chr19:39125438-39128519HeLa
SE_40594chr19:39125225-39128559Left_Ventricle
SE_42097chr19:39126229-39128147Lung
SE_48555chr19:39125255-39125967Right_Atrium
SE_50056chr19:39125256-39128091Sigmoid_Colon
SE_52339chr19:39125254-39126146Small_Intestine
SE_52339chr19:39126291-39128529Small_Intestine
SE_53291chr19:39125292-39126203Spleen
SE_53291chr19:39126576-39128320Spleen
SE_56725chr19:39125425-39126107VACO_400
SE_56725chr19:39126329-39127678VACO_400
SE_62811chr19:39125155-39186863Tonsil
SE_64225chr19:39126864-39127750NHEK
SE_65266chr19:39125298-39126341Pancreatic_islets
SE_65266chr19:39126385-39127265Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr193912615039126621
chr193912664639126984
Number: 1             
IDChromosomeStartEnd
GH19I038634chr193912486139129751
Enhancer Sequence
GAGTGGTGAC CCACGGCCTC GGGCTTTGGG GCTAAGGGGG TGCCCCTCAA GGGAGGCCGA 60
GGCAGGGGCC CAGAGGACCT GGGTAGATCT GCTCGTGTTC TGGGCTGGGA AGTCTGCACC 120
TGCCAGATTC CATTCACCTT GTGTCTTGGG GCTCCCGCCC AGGAGGAATA GCGGGGAGCT 180
GGGTGATCTT CCCTGGAACT TCTAGGCCCT GTGTCCTGCC CCATAGCACT CAGCAAGACT 240
TCCTGGGGCC CAGCGGGGCC TCACAGGGGG TCTCTGCACC CTTATTTGTC CCTGAGGCCT 300
GTCTCGTTGG CCATCTTTTA TTCTTGGGGT GCCCAAGCCT CATGTGCAGA CTTGGAATCC 360
GGTGAACAGT AGGAATCTTG ATTCTCTAGT TTGGGTGATT CCACATTTTT GTGCCTCAGT 420
TTTCTCATCT AAAAAATGGG GACGACTGCA ACAGTAACTA TGATAAACAC TGTGTAGGTC 480
CTTACACTTA CATCATTTGA TCCTCAGTTG CTAAATGATA TAAATAGTAT CATACCTACC 540
TCATGGCATC ATAAGTGTGA ATGCATGTAT AACACTTAGC AAAGAGCTAA GTGACCACAC 600
AGTTCATTAA ATGTTCATTA TGACCATCGT CTACACACAT GTAACTAACA CAGGCTCAAC 660
TGCTTGCTCA ACTAAAAAGA TTGCAGTGGC TACTCCGGCA GCGGGTGCTG CTTCACTGCC 720
GCTCATCATG GCACTGAGCA GATGTCCTGG AGCCAGGGAG AAAGGCACAG GCGGGCTGCT 780
GCCTTCATCC CGGGTCTCCC CCACCCGCTT GAGTGTGATT CAGGTGTTTT AAAGATGTGT 840
TTGGTACAAC GTGGTTTCTT AACACAAACC AGCTAATTTT GTACTTAACT GGGGAACAGC 900
ATTGAGCAGG CAGCCATCTG CGCACTTGCA GCCCGTGGTA TCTCACCTCT AAACGCCGCG 960
TGACTGCTGT GTCGGGGTTC TCAGTGAGAA CTCCAGCAAA AGATTCTGTA GTGAGGAAAG 1020
GGCCTCCTTT CTTCTCCCCT TTGGCTTCTG TTGCCCCACC CCACCTTCCT GACCTTTTAG 1080
GTCACAGGTG GAGAGGGCAG TGCTGAGTCA ACAAGGAAAA GGAGGAGGAA GGTGTGAATC 1140
TCAGGGAAGT AGGAGCCCAG CCCTGCCGGG GGAGTAGACG GGAGGGTTCC CTCTGTCTCA 1200
GTTCTGGCTC CATTGCTCTG TGTCCTGGGT CAAACAGGAT AGGTTCAAAA TACTCAGGAG 1260
GCTGAGGCAG GAGAATCACT 1280