EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS034-09133 
Organism
Homo sapiens 
Tissue/cell
ECC-1 
Coordinate
chr14:69280940-69282180 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gfi1bMA0483.1chr14:69281860-69281871AAATCACAGCC+6.02
Number of super-enhancer constituents: 54             
IDCoordinateTissue/cell
SE_00216chr14:69280056-69284487Adipose_Nuclei
SE_00958chr14:69280780-69283852Adrenal_Gland
SE_01773chr14:69279483-69284829Aorta
SE_02903chr14:69280154-69283720Bladder
SE_04320chr14:69279836-69284637Brain_Anterior_Caudate
SE_06376chr14:69279474-69285053Brain_Hippocampus_Middle
SE_07116chr14:69279651-69284457Brain_Hippocampus_Middle_150
SE_09974chr14:69280718-69284085CD14
SE_10217chr14:69278918-69284427CD19_Primary
SE_10927chr14:69278493-69285181CD20
SE_12450chr14:69278696-69284083CD3
SE_13798chr14:69280867-69283901CD34_Primary_RO01536
SE_19711chr14:69278919-69289914CD4p_CD25-_Il17p_PMAstim_Th17
SE_20000chr14:69278717-69284144CD56
SE_23287chr14:69280969-69282146Colon_Crypt_1
SE_23844chr14:69281021-69281554Colon_Crypt_2
SE_23844chr14:69281695-69282107Colon_Crypt_2
SE_25802chr14:69279829-69284554Duodenum_Smooth_Muscle
SE_26562chr14:69279542-69288565Esophagus
SE_27622chr14:69280610-69284176Fetal_Intestine
SE_28546chr14:69280384-69284209Fetal_Intestine_Large
SE_29562chr14:69277479-69284349Fetal_Muscle
SE_31416chr14:69280223-69284146Gastric
SE_34435chr14:69279712-69289129HCT-116
SE_37021chr14:69280774-69284450HSMMtube
SE_38917chr14:69280559-69284107IMR90
SE_40783chr14:69279886-69284110Left_Ventricle
SE_42151chr14:69279537-69284570Lung
SE_44214chr14:69280824-69284076NHDF-Ad
SE_44812chr14:69281004-69283795NHLF
SE_46115chr14:69280973-69284154Osteoblasts
SE_46691chr14:69280943-69281624Ovary
SE_46691chr14:69281626-69284104Ovary
SE_47482chr14:69280941-69281577Pancreas
SE_47482chr14:69281611-69282366Pancreas
SE_48168chr14:69280460-69284143Psoas_Muscle
SE_48639chr14:69279890-69284074Right_Atrium
SE_50069chr14:69279260-69284124Sigmoid_Colon
SE_51158chr14:69279858-69284542Skeletal_Muscle
SE_51840chr14:69280912-69283830Skeletal_Muscle_Myoblast
SE_52355chr14:69279406-69284222Small_Intestine
SE_53295chr14:69279232-69284176Spleen
SE_54538chr14:69278934-69287559Stomach_Smooth_Muscle
SE_55116chr14:69279941-69283956Thymus
SE_56951chr14:69281676-69282134VACO_400
SE_58723chr14:69255266-69284525Ly1
SE_59058chr14:69250411-69290070Ly3
SE_60370chr14:69257827-69284095Ly4
SE_60527chr14:69255025-69290272DHL6
SE_61098chr14:69252323-69292163HBL1
SE_61862chr14:69255096-69290190Toledo
SE_62217chr14:69237592-69290254Tonsil
SE_63619chr14:69280910-69284052HSMM
SE_65371chr14:69279532-69284462Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr146928132369281785
Number: 1             
IDChromosomeStartEnd
GH14I068811chr146927790069284695
Enhancer Sequence
GGGGTTCTGG AAGAAATCAA CATGCTACTA CAATGGAAGG CATTTGAAGG AAGTGGAAAG 60
TTTTCACAGA AAGTAGCCCA GAGACATGCA CAGAGTGCTG CTCTCTGTGC AGACCAGAAA 120
CCCCAAAGAT TTGTGCCTCT TTCTGTCAGA ATGCAGCTTT CTGGAGCCCA CCGGGCTATA 180
GAAGCTGCAT GGCGTCTGGA ATGGGAATGG GTTGGCCTAG TCTTCCCCTG GAGGTATGGA 240
GAGGAAAGGT GACACTTTCA GGCTTTGTGC AGGACAAGCA GAGAATATCA CTCAAATCCA 300
AGCTGGCTGC CCTGTGGGGG ACACAGGCCC ATGCCGGCAG GCCTGGGGAG AGCCACCGCT 360
TGCTGAGGTT AGGCCAGCAC CAGTGGGTGT GAGGAACCCA CCTCCAGTCT CAAGAGCAGG 420
GTTGGGCTTC CCTGGATGGG GAGGAAAGGG TTAAGCCGGC TTGGGCTCTG GAGGGAAAGC 480
ACTCGGCAGC TATAAACAGA GAGCCTAGGG AGGGAGGGGG CTGACAGGAT GTGGCCAGGG 540
CTCGAGCTGT CTGATTATTA ACTTCACTTT TATTTGGAGG GGGATTTGAT TCTCTGTTTT 600
ACTTCCCATC AAGGAAGTGA AAGCCCAGGT CTCAGAGGGG CCTGGTTTCA AATTGTTTTG 660
TCACAGCTCA TTTATTTTTC CTTTTAAATA AATAAACAAA ACCACCTCTT TGTTTTCCCC 720
TTAATGAGCA TTCAGCAAAT CATCTGTGGG TGAGGCATGA ACGGGGTTTT CTGGAGTCCT 780
TCATGGGAGA ACATTTGGCT TATTATTTTA AAAGGAAAAA GCAAGGATGT CTCCTTTAGC 840
TCCCAGTCTT CTCCAAGGCT GTGAAGGCAC TTTCTCTTTT GCCTCCTCTG AAATACCGAC 900
CTAGACCAGC GAGGAGTCTG AAATCACAGC CTCAAGCTCG GCCAAGGCCC CAGGAGCTTC 960
CTTGGTTGGA CCTTGGGGCT GGACCCGCAG CCTGCCATTC CATCTGACAG GCCCTGACCC 1020
TGAGGCCACG CAGAGGAAGC ACCCAGCACG GGCTCAGTGG TTTGTCTTCT TGCTTGGGCT 1080
CAGACCCATG GCTTTTGTTC CTCTGACACC CTGACATTTC TACTAAAATA ACAAAGCAAT 1140
TAAACACACA AAAGGATTCC ATGACAGCCT TAAAAAACAC CATTACATGT TCCTTTACCC 1200
AAGGTTGAAA ACATTTGGGA ACTTGATTTC CAACATCAAA 1240