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

TagContent
EnhancerAtlas ID
HS060-17820 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr19:39185130-39186800 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr19:39186290-39186308CTTTACTCCCTTCCTTCT-6.07
ZNF263MA0528.1chr19:39186013-39186034CTTTTTGCCTTTCCCTCCTCC-6.12
ZfxMA0146.2chr19:39185143-39185157CCCGCCTCGGCCTC+6.01
ZfxMA0146.2chr19:39185758-39185772CCCGCCTCGGCCTC+6.01
Number of super-enhancer constituents: 49             
IDCoordinateTissue/cell
SE_00117chr19:39182049-39186979Adipose_Nuclei
SE_00865chr19:39185510-39187918Adrenal_Gland
SE_01543chr19:39181993-39190228Aorta
SE_02408chr19:39181342-39185560Astrocytes
SE_03166chr19:39185728-39189384Brain_Angular_Gyrus
SE_03903chr19:39185394-39193508Brain_Anterior_Caudate
SE_04868chr19:39185423-39189876Brain_Cingulate_Gyrus
SE_05805chr19:39182078-39206004Brain_Hippocampus_Middle
SE_07777chr19:39185584-39193917Brain_Inferior_Temporal_Lobe
SE_09404chr19:39182333-39191485CD14
SE_20249chr19:39181278-39188425CD56
SE_22709chr19:39182642-39186831CD8_primiary
SE_23062chr19:39185118-39185515Colon_Crypt_1
SE_23062chr19:39185726-39186655Colon_Crypt_1
SE_23732chr19:39185140-39185416Colon_Crypt_2
SE_23732chr19:39185750-39186483Colon_Crypt_2
SE_24739chr19:39185106-39185492Colon_Crypt_3
SE_24739chr19:39185730-39186728Colon_Crypt_3
SE_25779chr19:39180965-39189795Duodenum_Smooth_Muscle
SE_26525chr19:39180697-39193852Esophagus
SE_27614chr19:39180632-39201469Fetal_Intestine
SE_28533chr19:39164445-39201888Fetal_Intestine_Large
SE_29583chr19:39185825-39186549Fetal_Muscle
SE_31384chr19:39185422-39186593Gastric
SE_34299chr19:39180509-39186508HCT-116
SE_35812chr19:39168616-39191950HMEC
SE_36926chr19:39172838-39186932HSMMtube
SE_38012chr19:39181151-39186650HUVEC
SE_40594chr19:39180727-39193965Left_Ventricle
SE_42097chr19:39180674-39193834Lung
SE_44161chr19:39181143-39185634NHDF-Ad
SE_44161chr19:39186536-39189303NHDF-Ad
SE_45660chr19:39180876-39186673Osteoblasts
SE_47114chr19:39164477-39226374Panc1
SE_47461chr19:39185655-39186661Pancreas
SE_48075chr19:39180646-39186770Psoas_Muscle
SE_48555chr19:39185073-39190229Right_Atrium
SE_50056chr19:39182445-39193963Sigmoid_Colon
SE_51136chr19:39181521-39186773Skeletal_Muscle
SE_51705chr19:39182066-39185548Skeletal_Muscle_Myoblast
SE_52339chr19:39180899-39193971Small_Intestine
SE_53291chr19:39181227-39190272Spleen
SE_54534chr19:39180651-39189737Stomach_Smooth_Muscle
SE_56725chr19:39185122-39189741VACO_400
SE_62811chr19:39125155-39186863Tonsil
SE_63494chr19:39182024-39185548HSMM
SE_64225chr19:39185744-39186682NHEK
SE_65266chr19:39181937-39187543Pancreatic_islets
SE_68725chr19:39186614-39190205H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr193918644739186795
chr193918563039186442
chr193918557039186200
Number: 1             
IDChromosomeStartEnd
GH19I038673chr193916453639206516
Enhancer Sequence
CTCAAGTGAT CCGCCCGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGGTG CGAGCCACTG 60
CGCCCGGCCC TGGCTGGGGG CTTCTTGACC TGACTCTGCT GTCTCTCCCT CACTGGCCAG 120
CACCTCCCAT TCTACTCAGA CATCGTGGAA TGAATGCCCA CCCCGTGTTT GTATGTATCA 180
TCTGTGTCTG TGTGACATTA AGCAAGTCAC TGAACCTCTC CCTGCCTCAG TTTCCTCATC 240
AAATGGAGAT ATATCGCATG TGATCATGGG GTTGGAGGTT TTAAAGAGTT GCTAATGTGT 300
AAATAGTAAG AACTAGCAAT TAGCCGTTAT AGCATAATTA CCTTTAATAT GTCATGCCCC 360
CCGCACCCCC GTGCTGAATG TAATTTTGCG GGGGGGCGGG TTGAGACAGG GTCTGGCTCT 420
GTCACCGAGG CTGGAGTGCA CTAACACAAT CTCAGCTTAC TGCAACCTCT GCCTCTCAGG 480
CACAAGCTGT CTTCCCACCT CAGCCTCTCG AGTAGCTGGG ACTACAGGCG CTCAGTACCA 540
CGCCTGGCTA ATTTTTGTAG TTTTTGTAGA GATGGGGTTT TGCCATGTTG CCTAGGCTGA 600
TCTCAAACTC CTGTGCTAAA GCAATCCTCC CGCCTCGGCC TCCTAAAGTG CTGGGATTAC 660
ATGGTGTGTG CCACCATGCC TGGCTGGCCA GAATGTAAAT GATAACTGTT TTGCTTCCTC 720
CTGTGTCCAG TACATAATAG GGCTCCAAGT CAGTATTTGT GAGGCAGGTG CATGCCTCTT 780
AGTTGCGGTC CTGAGGGCAT GGCCACTGCC ACGTTCTGGA CAGTCAGAGT CGCTGCTGCC 840
CCTGGAAGAT GACCGCGATC ATGAAGCCCA GGAGAGCTCG ATGCTTTTTG CCTTTCCCTC 900
CTCCCACAGA GGGCTGGCAG CTCTGGTTCC TCCCAAATGA AATAGAAACC TTGAGTTTGC 960
ATTTCTTCTT TGGCGTGCCG GCAGGGCACC TCTGCCTTCC TCTTCCTGCC AGGGGGAGGA 1020
AGTTTCTCTC AGGGGCTCTT CACCCTGCTT TATTCCTGGC CATCACACAT TGACCCTTGT 1080
CCCCTTCGGC TCTTTCCCTG CATGGCAGGG ACAGCATGAC CGTTTAATGG CTTTGTGAGG 1140
CCAGCATGCC AGCCTCACTT CTTTACTCCC TTCCTTCTCG GAGTGGGCTC TGTCCCTTCT 1200
GCAGGAGGGC TTTGGCACAT GCTCTTCCCA GTATCTGGAA GGTCTCCCTC ATTTTTATCT 1260
TATTAACTCC TCATCCTTCA GCTCAGAGTT TGAGAATGAC TTCTTCAAGG ACACCTTTCT 1320
GTGTCTGCCT CACCAGTCGC TTGGTGCCCC CCCACCCCGC CACCATGCTG ACCGCACTCT 1380
TCAGCTCCCA TCCCAGGGGA GGTGACACAA ACTCGGCCCC AGGAGCCCAG CACCTGGCTT 1440
TAAACCCAGC TCTGTAACTT TCTAGGTGTG TGACTGATGG GAGCAAGCCA CTTCACCTCT 1500
CAGGCCCTCC GTTTCCTCAT CTGCAAAATG GAGGCAGTAC TAGCACCTCC CTCCAGAGAT 1560
GATTACGAGG GTGACAGAAT TAGTAAGTGA CCAAGTGCCT CGAGCAGTGC CCGCCCCTAG 1620
TAGACTCTAT GGAAGTGTCT GCTGCAGTTA TTGCTGTTAT TATTACCACT 1670