EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS040-17926 
Organism
Homo sapiens 
Tissue/cell
Esophagus 
Coordinate
chr19:11205010-11207740 
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUN(var.2)MA0489.1chr19:11205882-11205896AAGAAATGAGTCAT+7.12
JUN(var.2)MA0489.1chr19:11207063-11207077ATGACTCATTTCTT-7.12
JUN(var.2)MA0489.1chr19:11207058-11207072AGGAAATGACTCAT+8.12
JUN(var.2)MA0489.1chr19:11205887-11205901ATGAGTCATTTCCT-8.12
SREBF1MA0595.1chr19:11205756-11205766GTGGGGTGAT-6.02
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_01022chr19:11203682-11206319Adrenal_Gland
SE_01022chr19:11206333-11207663Adrenal_Gland
SE_12085chr19:11204949-11207773CD3
SE_14622chr19:11198676-11207877CD4_Memory_Primary_7pool
SE_17142chr19:11204971-11207608CD4p_CD225int_CD127p_Tmem
SE_19715chr19:11204867-11207840CD4p_CD25-_Il17p_PMAstim_Th17
SE_20994chr19:11198676-11207604CD8_Memory_7pool
SE_22774chr19:11204855-11208057CD8_primiary
SE_23239chr19:11203891-11206070Colon_Crypt_1
SE_23239chr19:11206100-11207601Colon_Crypt_1
SE_24095chr19:11204989-11205979Colon_Crypt_2
SE_24095chr19:11206366-11207012Colon_Crypt_2
SE_24095chr19:11207130-11207564Colon_Crypt_2
SE_24928chr19:11205061-11206082Colon_Crypt_3
SE_24928chr19:11206201-11206876Colon_Crypt_3
SE_26902chr19:11204916-11207828Esophagus
SE_28429chr19:11198835-11207741Fetal_Intestine
SE_29308chr19:11199027-11207595Fetal_Intestine_Large
SE_29905chr19:11204956-11208148Fetal_Muscle
SE_31737chr19:11204927-11207763Gastric
SE_34726chr19:11198191-11208606HeLa
SE_36050chr19:11204941-11207563HMEC
SE_38264chr19:11198668-11208150HUVEC
SE_40068chr19:11198411-11207591K562
SE_42817chr19:11199051-11207805Lung
SE_44493chr19:11205013-11206118NHDF-Ad
SE_44493chr19:11206328-11207705NHDF-Ad
SE_44932chr19:11205113-11207883NHLF
SE_47693chr19:11204994-11205972Pancreas
SE_47693chr19:11206368-11206786Pancreas
SE_47693chr19:11207237-11207566Pancreas
SE_49361chr19:11205119-11206191Right_Atrium
SE_49361chr19:11206197-11207709Right_Atrium
SE_50772chr19:11198863-11207767Sigmoid_Colon
SE_52540chr19:11198883-11208401Small_Intestine
SE_54059chr19:11198844-11207806Spleen
SE_57847chr19:11205007-11205595VACO_503
SE_64571chr19:11204940-11207695NHEK
SE_65732chr19:11198652-11207882Pancreatic_islets
SE_68998chr19:11207123-11207544H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr191120695311207150
chr191120569611206011
chr191120634811207740
Enhancer Sequence
GGTTTCTCCA CATTGGTTCA GGCTGTTCTC GAACTCCCAA CCTCAGGTGA TCCACCCGCC 60
TCAGCCTCCC AAAGTGCTGG GATTATAGGC GTGAGCCCCC GAACCCGGCC ACTCCCAGCT 120
AAGTTTAAAT TTTTTGTTTG TTTGTTCGTT TGTTTTTATT TTTTGAGACA GAGTCTCCCG 180
CCCAGGCTGG AGCGCAGATC ACTGCATCCT TGACCTCCCA GGCTTAAGCC ATCCTCCCCA 240
CTCAGCCTCC CAAGTAGCTG GGATTACAGG TGTGTGCCAC TATGCTTGGC TAAGTTGTGT 300
ATTTTTTGTA GAGATGGGGT TCAAGGGATT CTCGCTTTGT TGCCTCGGTT GGTCTCAAAC 360
TCCTGGGCTC AAGCAGTCCT CCCTCCTCAG CCTCCCAAGG TGCTGGGGAA ATCCACTTTT 420
GAAACATTGT CTGGAGAGTT GCCCAGGTGG TAGATCACAG AAATAGGTCA TCGTGGGGTC 480
CTTCCCATGG GTGCAGTCTT GAGCCACCTG TGGCCAGCAA ATATTTGGAG AATAATAGTC 540
AGGGGAGAGC TTGAGGTCCA GGGAAAGGTT TTGTTTTTCT TCAGGGAAAG GTTTTTATTG 600
TTCTTTATCC CTCCTTAAAG GACCTTCAGG TGTTACTGAC ATTCCCGGTC TACCCAGTGG 660
CACATTTAGT TTGTAAGCTG GGCCCTCGTA CAGAGGTAGG GAGGTGAGAG CATTGGATTA 720
GTGGTCACCA AAGCTGCGGT CACCTAGTGG GGTGATCAGA GGCTCCTCCC TTAAGATCTT 780
GATTGCCAAC GCCTCTGGCC CAACTTTCCT TTTTATTTAT CGCAAGCCTC CTGGAATCTC 840
AATTGCTTTT TGCCCACCCG GTGTGTCAGC ACAAGAAATG AGTCATTTCC TCCTTTAAGC 900
ACAGTTGAAA TTGAGCTGTG AGTCAGTGAG GTGTGTACGA TATTGTCAAA GCGGGGTGTG 960
TACAGTATTG ACAGATCTGT AGTTGGGCAA GAGAATTATC AGAGTTTGTG ACCACAGCAG 1020
ATTCCAAAGC TCGACTCATT TTCTTCTCTC TTCCTTCCCT TTTTTCTTTT CTTTTTTTTT 1080
TTTTTTTTGA CAGAGTCTCG CTCTGTTGCC CAGGCTGGAG TGCAGTGGCA CAATCTGGGC 1140
TCACTGCAGC CCCTGCCTCC TGGGTTCAAA TGATTCTCAT GTTTCAGCCT CCCGAGTAGC 1200
TGCAATTACA GGCATTCGGG TTCAAGTGAT TCTCCTGCCT CAGCCACCTG AGCAGCTGGG 1260
ATTACAGGCG CCCGCCACCA CGCCCGGCTA ATTTTTGTAT TTTTAGTAGA GACGGGGTTT 1320
CACCATGTTG GCCAGGCTGG TCTCGAACTC CTGAACTCAG GTGATCCGCC CACTTCGGCC 1380
TCCCAAAGTG CTGAGATTAC AGACGTGAGT CACCGCGCCC AGCCTGTTCT GTTCTTTAAT 1440
TCTCAAAACA CCCTCTAGGA AGTAGAGACT GCCATTCTCC CCCATTTTAC AGATCAGGAA 1500
ACTGAGTCCC AGAAGGATTT AGTCAGTTAC CCAAGTTGTT CTAGTTAAAT GGCCTGGAAA 1560
GCCAGTGAAG CCCAGGATTG TCTATCTAAC CCCCTTACTA CTCTAACTTT CAGGGAATCC 1620
ACATGAATGT GCTGGGTCAA CCATCAAAGT TGAAATGGAT AAAGGGGGCT GGATGCGGTG 1680
GCTGATGCCT GTAATCCTAG CACTTTGGGA GGCCGAGATG GGTGGGTGGA TTGCTTGAGC 1740
CCAAGAGTTT GAGACCAGCC TGGGCAACAT AGTGAGACAC CTGTCTCTGC AAAAAATAAA 1800
TAAAAAGTTA GCTGAGTGTG ATGGTGCACC CCTCTAGTCA CAGCTGTTGA GTTAGGCTTA 1860
GGCAGGAGGA TCGCATGAAC CTGGGAGGTG GAGGCGGCCG TGAGCCTCAG TCATGCCACT 1920
GCACTCCAAC CTGGGCAACA GAGTGAAAGC CGGTGTCCGA AAGAGAAAGA AAAAAAGACA 1980
TAGATACATC TTTTAAAGTT AGGTTGTATG TTAATTACCT ACAACTCAGT TTCAACTGTG 2040
CTTAAAGGAG GAAATGACTC ATTTCTTGCT ACATATCAAA TTAGCCCAAA ATGTAGTGGC 2100
TTAAAACAAC ACATTTATGA TTTCTCAGTT TTTGCGTGTC AGGAATTTGG AAGCAGCACA 2160
GCTAGACGGT TCCAGCTCAG GGTCTCTCAT GAAGTTGCAA TCAAAATATT GGCAGGAGAG 2220
AAAAACATAT TTTCAGAAGC TGCAGGCATA GGAAGACTTG GCTGGGGTTG AAGGATCCAC 2280
TTCCAAGATG GCGCACTCAG TGGCTCTTGG CTGGAGGCCT CAGTTCCCTG CTGCGTGGAG 2340
CTCTCCCTCC AGCTGCTTGA GTGGACTCAT GACATGCAGC TGGCCTCCCC TGGAGCAGTC 2400
GATCCAACAA TGAGCATGGC CATGAACTAG GCTCAGAAGC CACTCCCTGT CGTCTCTACA 2460
TTTTCCTATC AGAAGCAAGT CATTAAAAGT CCAGTGCCAC TCCAGGGGAG ACGAATTAGG 2520
CTCTGCCTTC TGAAAGGATT ATCACAGAAG ATGCGGTCCT ATATTCTTTT TTTAAAATTA 2580
TTCTTTTTTT TATTTTGTAG AGATGGGGTC TTGGTATGTT GCCTAGGCCA GTCTGGAATT 2640
CCTGGGCTCA AACAATCCTG TCTCTGCCTC CCAAAGTGTT GGGATTACAG GCATGAGCCA 2700
CTGCACCTGG TCATGTGGTC ATATTTTCTT 2730