EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS145-11746 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr19:39174090-39175530 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs973009chr1939174332hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SRFMA0083.3chr19:39174375-39174391TGCCCATATAAGGCAA-6.43
SRFMA0083.3chr19:39174375-39174391TGCCCATATAAGGCAA+7.04
STAT1MA0137.3chr19:39175026-39175037TTTCCTAGAAA-6.14
Number of super-enhancer constituents: 65             
IDCoordinateTissue/cell
SE_00117chr19:39172768-39180290Adipose_Nuclei
SE_00865chr19:39172709-39178176Adrenal_Gland
SE_01543chr19:39172839-39177657Aorta
SE_02408chr19:39172990-39177649Astrocytes
SE_02946chr19:39173560-39175782Bladder
SE_03166chr19:39174301-39175014Brain_Angular_Gyrus
SE_03903chr19:39172941-39177792Brain_Anterior_Caudate
SE_04868chr19:39173279-39175506Brain_Cingulate_Gyrus
SE_05805chr19:39172836-39178090Brain_Hippocampus_Middle
SE_06803chr19:39173207-39177647Brain_Hippocampus_Middle_150
SE_07777chr19:39173597-39177838Brain_Inferior_Temporal_Lobe
SE_08790chr19:39174651-39174897Brain_Mid_Frontal_Lobe
SE_09404chr19:39164511-39180526CD14
SE_13194chr19:39173530-39174621CD34_Primary_RO01480
SE_13490chr19:39171584-39177811CD34_Primary_RO01536
SE_14624chr19:39172843-39178692CD4_Memory_Primary_7pool
SE_19537chr19:39173158-39178239CD4p_CD25-_Il17p_PMAstim_Th17
SE_20249chr19:39164561-39178319CD56
SE_20865chr19:39170480-39179166CD8_Memory_7pool
SE_22709chr19:39169957-39177919CD8_primiary
SE_23062chr19:39172808-39177650Colon_Crypt_1
SE_23732chr19:39172948-39175688Colon_Crypt_2
SE_24739chr19:39172745-39175747Colon_Crypt_3
SE_25779chr19:39164448-39177989Duodenum_Smooth_Muscle
SE_26525chr19:39172863-39178234Esophagus
SE_27614chr19:39164407-39180553Fetal_Intestine
SE_28533chr19:39164445-39201888Fetal_Intestine_Large
SE_29583chr19:39173105-39177586Fetal_Muscle
SE_31384chr19:39172828-39178145Gastric
SE_34299chr19:39171460-39178238HCT-116
SE_34681chr19:39170836-39180506HeLa
SE_35430chr19:39173018-39177757HepG2
SE_35812chr19:39168616-39191950HMEC
SE_36926chr19:39172838-39186932HSMMtube
SE_38012chr19:39172846-39178074HUVEC
SE_38896chr19:39172978-39177574IMR90
SE_40018chr19:39173109-39177708K562
SE_40594chr19:39164568-39178326Left_Ventricle
SE_41601chr19:39173026-39175372LNCaP
SE_42097chr19:39171618-39178328Lung
SE_44161chr19:39172957-39177683NHDF-Ad
SE_44797chr19:39173417-39177160NHLF
SE_45660chr19:39172827-39180503Osteoblasts
SE_46686chr19:39173697-39175316Ovary
SE_47114chr19:39164477-39226374Panc1
SE_47461chr19:39172966-39175743Pancreas
SE_48075chr19:39168529-39178289Psoas_Muscle
SE_48555chr19:39172970-39178180Right_Atrium
SE_49449chr19:39173064-39175397Right_Ventricle
SE_50056chr19:39172842-39178237Sigmoid_Colon
SE_51136chr19:39172773-39177883Skeletal_Muscle
SE_51705chr19:39173163-39177229Skeletal_Muscle_Myoblast
SE_52339chr19:39168564-39178308Small_Intestine
SE_53291chr19:39172716-39177734Spleen
SE_54534chr19:39172958-39177716Stomach_Smooth_Muscle
SE_55638chr19:39173251-39174352Thymus
SE_55638chr19:39174378-39175365Thymus
SE_56725chr19:39172594-39175708VACO_400
SE_57359chr19:39173016-39175736VACO_503
SE_58038chr19:39172904-39175754VACO_9m
SE_62811chr19:39125155-39186863Tonsil
SE_63494chr19:39172985-39177528HSMM
SE_64225chr19:39172977-39177763NHEK
SE_65266chr19:39168886-39178027Pancreatic_islets
SE_68725chr19:39172837-39175413H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr193917500039175365
Number: 1             
IDChromosomeStartEnd
GH19I038673chr193916453639206516
Enhancer Sequence
AGGCCCCGTG AACAGAGGAG GGGTCTGAGC CAGGCCTCCT AGGCCATTGG TGGGAGGGAG 60
AATGAGACAG CCATTTGGCC CACAGGCCAC CAACTTTTCC CCCCCTTCTC TAAAAGACAC 120
ACAATGGCAG TTGGGCTGCA CCTTTGTGAG TCACCGGTGA TAGCCCATCA TAAATTGTTA 180
TTTCCTATAT TTCCAGAGCA GCTTTATCGG GCGTTGCCTG TGCAGTCCGG GAACCGATTT 240
GGTATGGGGT CAGTTAACAT GCTGTCTTGT TGAAATCTGT CATCATGCCC ATATAAGGCA 300
AACTCCTTGG ATTACTTTTT ACCTTGGCAG AATCACAGGA ATGTCAAGGT AACCAGGCCA 360
CCTCAGCATA GCTCTGATTC TCACCCGGTC ACCTGACTTG CCCGCCCTCC CCCATGACTC 420
ACCCAGTGGC TCAGCATGGG GCCTGCTGCA CTGTGGCTGC TGGAATCTGC CAAGGACCTC 480
CTGGGACTGC CCTTGGTTTT GTGTCTTCCT TAGAGTAGAT CAAATGAGAG GAACCATGTG 540
AAGTAGCTCA CACAGGGCCT AACAGAGCAA ACACAAGACG TGGAAAGCAG ACTTGGTGAG 600
GCTTGAGTTT AGTTTGGGGG TTGCGGGGGT CCCAGCTCTG CTGCTTAACA GCCCTGTGGC 660
CATGGGTATA TCCCCCAGCA TTCAGAGCCT TATCTGTAAA ATTAGAGCAC GCAGAACAAA 720
CCCTGGTACA CACTAAGTGC TCAATAAATG TGAGTCATTT GTGTAATTAT AGTAGGGTAG 780
GCCTTATGCC CCACCCAGTC ATAAAAATGC CTCTTGCTGT TGTTGGTTCA GGCTCAGCCC 840
CTTAGTGGCT TTCATGGGGC AGGTTGACAT GGTACCCAGA GTCCTCCTCG GTCCTCTTCC 900
CATGGTGTAG TGAGAGCACT CAGGACCACC TAGGCCTTTC CTAGAAAACT GAACCCACAC 960
CTTCCCAGTG CTGCCCCACC CTGGTCCCCC ACCCCCTGCA GGACAAACCA CTCCTCCCTT 1020
GTTTTGGGGC CAGGAGTCAG ATCTGCCCCT GAGAGCAGCA GGGGCCCCTT TGTCCTTTGA 1080
CGTCATACCC ACACCGCTCC TGGAGACAGC CACCCCTTCA TGCCAGCCCC AGGAAGGCTT 1140
GTAGGTGGGG CGAGCCAGGG TGAGAGTGTA GCCCTGTTCC TCGGCCAGGG CAGATGTTTC 1200
ACCATTTTTA ATGGAGCAAT TATGAGTCAG AGGTTTCAGT CTCTACTGGT TCCTCCCGAT 1260
CCTATAATTA CTCTTTGGCT ATAGAATCCT ATTTTGATCT CTTCTTTTCT TTTCTCTTCT 1320
TTCTCTCTCT GTGGTCATGG TCAGGTTTTT CTTTTTTTAA ATCCTCCCAA GACACTGCTA 1380
ATGTTGTCTG TCTCATGCAT CCAAGGAATC TGAGATGGAC TGAATATTGT CAAGGGAAAA 1440